This article is about congenital disorders in humans. For animals, see Teratology.
| Congenital disorder |
| Classification and external resources |
| Specialty |
Medical genetics, pediatrics |
| DiseasesDB |
28811 |
| MeSH |
D009358 |
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[edit on Wikidata]
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Congenital disorder, also known as congenital disease, birth defect or anomaly,[1] is a condition existing at or before birth regardless of cause. Of these diseases, those characterized by structural deformities are termed "congenital anomalies" and involve defects in a developing fetus. Birth defects vary widely in cause and symptoms. Any substance that causes birth defects is known as a teratogen. Some disorders can be detected before birth through prenatal diagnosis (screening).
Birth defects may be the result of genetic or environmental factors. This includes errors of morphogenesis, infection, epigenetic modifications on a parental germline, or a chromosomal abnormality. The outcome of the disorder will depend on complex interactions between the pre-natal deficit and the post-natal environment.[2] Animal studies indicate that the mother's (and likely the father's) diet, vitamin intake, and glucose levels prior to ovulation and conception have long-term effects on fetal growth and adolescent and adult disease.[3] Animal studies have shown that paternal exposures prior to conception and during pregnancy result in increased risk of certain birth defects and cancers. This research suggests that paternal food deprivation, germ line mutations, alcohol use, chemical mutagens, age, smoking habits and epigenetic alterations can affect birth outcomes.[4][5][6][7] However, the relationship between offspring health and paternal exposures, age, and lifestyle are still relatively weak. This is likely because paternal exposures and their effects on the fetus are studied far less extensively than maternal exposures.
Birth defects are present in about 3% of newborns in USA.[8] Congenital anomalies resulted in about 632,000 deaths per year in 2013 down from 751,000 in 1990.[9] The type with the greatest numbers of deaths are congenital heart disease (323,000), followed by neural tube defects (69,000).[9]
Contents
- 1 Classification
- 1.1 Primarily structural[10]
- 1.1.1 Terminology
- 1.1.2 Examples of primarily structural congenital disorders
- 1.2 Primarily metabolic
- 1.3 Other
- 2 Causes
- 2.1 Fetal alcohol exposure
- 2.2 Toxic substances
- 2.2.1 Medications and supplements
- 2.2.2 Environmental toxical substances
- 2.3 Paternal smoking
- 2.4 Infections
- 2.5 Lack of nutrients
- 2.6 Physical restraint
- 2.7 Genetic causes
- 2.8 Socioeconomic status
- 2.9 Role of radiation
- 2.10 Father's age
- 2.11 Unknown or multifactorial
- 3 Epidemiology
- 4 See also
- 5 References
- 6 External links
Classification
Much of the language used for describing congenital conditions predates genomic mapping, and structural conditions are often considered separately from other congenital conditions. It is now known that many metabolic conditions may have subtle structural expression, and structural conditions often have genetic links. Still, congenital conditions are often classified in a structural basis, organized when possible by primary organ system affected.
Primarily structural[10]
Several terms are used to describe congenital abnormalities. (Some of these are also used to describe noncongenital conditions, and more than one term may apply in an individual condition.)
Terminology
- A congenital physical anomaly is an abnormality of the structure of a body part. An anomaly may or may not be perceived as a problem condition. Many, if not most, people have one or more minor physical anomalies if examined carefully. Examples of minor anomalies can include curvature of the 5th finger (clinodactyly), a third nipple, tiny indentations of the skin near the ears (preauricular pits), shortness of the 4th metacarpal or metatarsal bones, or dimples over the lower spine (sacral dimples). Some minor anomalies may be clues to more significant internal abnormalities.
- Birth defect is a widely used term for a congenital malformation, i.e. a congenital, physical anomaly which is recognizable at birth, and which is significant enough to be considered a problem. According to the CDC, most birth defects are believed to be caused by a complex mix of factors including genetics, environment, and behaviors,[2] though many birth defects have no known cause. An example of a birth defect is cleft palate, which occurs during the fourth and seventh week of gestation.[11] Body tissue and special cells from each side of the head grow toward the center of the face. They join together to make the face.[11] A cleft means a split or separation; the " roof" of the mouth is called the palate.[12]
- A congenital malformation is a congenital physical anomaly that is deleterious, i.e. a structural defect perceived as a problem. A typical combination of malformations affecting more than one body part is referred to as a malformation syndrome.
- Some conditions are due to abnormal tissue development:
- A malformation is associated with a disorder of tissue development.[13] Malformations often occur in the first trimester.
- A dysplasia is a disorder at the organ level that is due to problems with tissue development.[13]
- It is also possible for conditions to arise after tissue is formed:
- A deformation is a condition arising from mechanical stress to normal tissue.[13] Deformations often occur in the second or third trimester, and can be due to oligohydramnios.
- A disruption involves breakdown of normal tissues.[13]
- When multiple effects occur in a specified order, it is known as a sequence. When the order is not known, it is a syndrome.
Examples of primarily structural congenital disorders
A limb anomaly is called a dysmelia. These include all forms of limbs anomalies, such as amelia, ectrodactyly, phocomelia, polymelia, polydactyly, syndactyly, polysyndactyly, oligodactyly, brachydactyly, achondroplasia, congenital aplasia or hypoplasia, amniotic band syndrome, and cleidocranial dysostosis.
Congenital anomalies of the heart include patent ductus arteriosus, atrial septal defect, ventricular septal defect, and tetralogy of fallot. Helen Taussig has been a major force in research on congenital anomalies of the heart.[14]
Congenital anomalies of the nervous system include neural tube defects such as spina bifida, meningocele, meningomyelocele, encephalocele and anencephaly. Other congenital anomalies of the nervous system include the Arnold-Chiari malformation, the Dandy-Walker malformation, hydrocephalus, microencephaly, megencephaly, lissencephaly, polymicrogyria, holoprosencephaly, and agenesis of the corpus callosum.
Congenital anomalies of the gastrointestinal system include numerous forms of stenosis and atresia, and perforation, such as gastroschisis..
Congenital anomalies of the kidney and urinary tract (CAKUT) include renal parenchyma, kidneys, and urinary collecting system.[15]
Defects can be bilateral or unilateral, and different defects often coexist in an individual child
Primarily metabolic
Main article: inborn error of metabolism
A congenital metabolic disease is also referred to as an inborn error of metabolism. Most of these are single gene defects, usually heritable. Many affect the structure of body parts but some simply affect the function.
Other
Other well defined genetic conditions may affect the production of hormones, receptors, structural proteins, and ion channels.
Causes
Fetal alcohol exposure
Main articles: Fetal alcohol spectrum disorder and Fetal alcohol syndrome
The mother's consumption of alcohol during pregnancy can cause a continuum of various permanent birth defects : cranofacial abnormalities,[16] brain damage,[17] intellectual disability,[18] heart disease, kidney abnormality, skeletal anomalies, ocular abnormalities.[19]
The prevalence of children affected is estimated at least 1 percent in U.S.[20] as well in Canada.
Very few studies have investigated the links between paternal alcohol use and offspring health.[5]
However, recent animal research has shown a correlation between paternal alcohol exposure and decreased offspring birth weight. Behavioral and cognitive disorders, including difficulties with learning and memory, hyperactivity, and lowered stress tolerance have been linked to paternal alcohol ingestion. The compromised stress management skills of animals whose male parent was exposed to alcohol are similar to the exaggerated responses to stress that children with Fetal Alcohol Syndrome display because of maternal alcohol use. These birth defects and behavioral disorders were found in cases of both long- and short-term paternal alcohol ingestion.[21][4] In the same animal study, paternal alcohol exposure was correlated with a significant difference in organ size and the increased risk of the offspring displaying ventricular septal defects (VSD) at birth.[4] VSD has also been correlated with paternal alcohol abuse in humans.[22]
Toxic substances
Further information: Developmental toxicity, Drugs in pregnancy and Environmental toxins and fetal development
Substances whose toxicity can cause congenital disorders are called "teratogens", and include certain pharmaceutical and recreational drugs in pregnancy as well as many environmental toxins in pregnancy.[citation needed]
A review published in 2010 identified 6 main teratogenic mechanisms associated with medication use: folate antagonism, neural crest cell disruption, endocrine disruption, oxidative stress, vascular disruption and specific receptor- or enzyme-mediated teratogenesis.[23]
It is estimated that 10% of all birth defects are caused by prenatal exposure to a teratogenic agent.[24] These exposures include, but are not limited to, medication or drug exposures, maternal infections and diseases, and environmental and occupational exposures. Paternal smoking use has also been linked to an increased risk of birth defects and childhood cancer for the offspring, where the paternal germ line undergoes oxidative damage due to cigarette use.[25][26] Teratogen-caused birth defects are potentially preventable. Studies have shown that nearly 50% of pregnant women have been exposed to at least one medication during gestation.[27] During pregnancy, a female can also be exposed to teratogens from the contaminated clothing or toxins within the seminal fluid of a partner.[7][21][28] An additional study found that of 200 individuals referred for genetic counseling for a teratogenic exposure, 52% were exposed to more than one potential teratogen.[29]
Medications and supplements
The most notorious teratogenic drug is the thalidomide, developed at the end of 1950 by Chemie Grűnenthal as a hypnotic and antiemetic and therefore frequently prescribed to pregnant women in almost 50 countries worldwide between 1956- 1962.[30] Until William McBride published the study leading to its withdrawal from the market at 1961, about 8- 10 000 severely malformed children were born. The most typical disorder induced by thalidomide were reductional deformities of the long bones of the extremities (phocomelia), otherwise a rare deformity, which therefore helped to recognise the teratogenic effect of the new drug. Among other malformations caused by thalidomide were those of ears, eyes, brain, kidney, heart, digestive and respiratory tract. 40% of the prenatally affected children died soon after birth.[30] As thalidomide is used today as a treatment for multiple myeloma and leprosy, several births of affected children were described in spite of the strictly required use of contraception among female patients treated by it.
Vitamin A, or retinol, is the sole vitamin which is embryotoxic even in a therapeutic dose, for example in multivitamins, because its metabolite, the retinoic acid, plays an important role as a signal molecule in the development of several tisues and organs. Its natural precursor, the β-carotene, is considered safe, whereas the consumption of animal liver can lead to malformation (liver stores lipofile vitamines including retinol).[30] Isotretinoin (13-cis-retinoic-acid; brand name Roaccutane), vitamine A analog, which is often used to treat severe acne, is such a strong teratogen that just a single dose taken by a pregnant woman (even transdermally) may result in serious birth defects. Because of this effect, most countries have systems in place to ensure that it is not given to pregnant women, and that the patient is aware of how important it is to prevent pregnancy during and at least one month after treatment. Medical guidelines also suggest that pregnant women should limit vitamin A intake to about 700 μg/day, as it has teratogenic potential when consumed in excess.[31][32] Vitamine A and similar substances can induce spontaneous abortions, premature births, defects of eyes (microphthalmia), ears, thymus, face deformities, neurological (hydrocephalus, microcephalia) and cardiovascular defects, as well as mental retardation.[30]
Tetracycline, an antibiotic, should never be prescribed to women in the reproductive age or children, because of its negative impact on bone mineralization and teeth mineralization. The "tetracycline teeth" have brown or grey colour as a result of a defective development of both the dentine and the enamel of teeth.[30]
Several anticonvulsants are known to be highly teratogenic. Phenytoin, also known as diphenylhydantoin, along with carbamazepine is responsible for the fetal hydantoin syndrome, which may typically include broad nose base, cleft lip and/or palate, microcephalia, nails and fingers hypoplasia, intrauterine growth restriction and mental retardation. Trimethadione taken during pregnancy is responsible for the fetal trimethadione syndrome, characterized by craniofacial, cardiovascular, renal and spine malformations, along with a delay in mental and physical development. Valproate has anti-folate effects, leading to neural tube closure-related defects such as spina bifida. Lower IQ and autism have recently also been reported as a result of intrauterine valproate exposure.[30]
Hormonal contraception is considered as harmless for the embryo. Peterka and Novotná[30] do however state that syntethic progestines used to prevent miscarriage in the past frequently caused masculinization of the outer reproductive organs of female newborns due to their androgenic activity. Diethylstilbestrol is a synthetic estrogen used from the 1940s to 1971 when the prenatal exposition has been linked to the clear-cell adenocarcinoma of the vagina. Following studies showed elevated risks for other tumors and congenital malformations of the sex organs for both sexes.
All cytostatics are strong teratogenes, abortion is usually recommended when pregnancy is found during or before chemotherapy. Aminopterin, a cytostatic drug with anti-folate effect, was used during the 1950s and 1960s to induce therapeutic abortions. In some cases the abortion didn´t happen, but the newborns suffered a fetal aminopterin syndrome consisting of growth retardation, craniosynostosis, hydrocephalus, facial dismorphities, mental retardation and/or leg defomities[30][33]
Environmental toxical substances
Drinking water is often a vessel through which harmful toxins travel. Studies have shown that heavy metals, elements, nitrates, nitrites, fluoride can be carried through water and cause congenital disorders.
Nitrate, which is found mostly in drinking water from ground sources, is a powerful teratogen. A case-control study in rural Australia that was conducted following frequent reports of prenatal mortality and congenital malformations found that those who drank the nitrate-infected groundwater, as opposed to rain water, ran the risk of giving birth to children with central nervous system disorders, muscoskeletal defects, and cardiac defects.[34]
Chlorinated and aromatic solvents such as benzene and trichloroethylene sometimes enter the water supply due to oversights in waste disposal. A case-control study on the area found that by 1986, leukemia was occurring in the children of Woburn, Massachusetts at a rate that was four times the expected rate of incidence. Further investigation revealed a connection between the high occurrence of leukemia and an error in water distribution that delivered water to the town with significant contamination manufacturing waste containing trichloroethylene.[35] As an endocrine disruptor, the DDT was shown to induce miscarriages, interfere with the development of the female reproductive system, cause the congenital hypothyroidism and suspectibly childhood obesity.[30]
Fluoride, when transmitted through water at high levels, can also act as a teratogen. Two reports on fluoride exposure from China, which were controlled to account for the education level of parents, found that children born to parents who were exposed to 4.12 PPM fluoride grew to have IQs that were, on average, seven points lower than their counterparts whose parents consumed water that contained 0.91 PPM fluoride. In studies conducted on rats, higher PPM fluoride in drinking water lead to increased acetylcholinesterase levels, which can alter prenatal brain development. The most significant effects were noted at a level of 5 PPM.[36]
The fetus is even more susceptible to damage from carbon monoxide intake, which can be harmful when inhaled during pregnancy, usually through first or second-hand tobacco smoke. The concentration of carbon monoxide in the infant born to a non-smoking mother is around 2%, and this concentration drastically increases to a range of 6%-9% if the mother smokes tobacco. Other possible sources of prenatal carbon monoxide intoxication are exhaust gas from combustion motors, use of dichloromethane (paint thinner, varnish removers) in enclosed areas, defective gas hot water heaters, indoor barbeques, open flames in poorly-ventilated areas, atmospheric exposure in highly polluted areas. Exposure to carbon monoxide at toxic levels during the first two trimesters of pregnancy can lead to intrauterine growth restriction, leading to a baby that has stunted growth and is born smaller than 90% of other babies at the same gestational age. The effect of chronic exposure to carbon monoxide can depend on the stage of pregnancy in which the mother is exposed. Exposure during the embryonic stage can have neurological consequences, such as telencephalic dysgenesis, behavioral difficulties during infancy, and reduction of cerebellum volume. There are also possible skeletal defects that could result from exposure to carbon monoxide during the embryonic stage, such as hand and foot malformations, hip dysplasia, hip subluxation, agenisis of a limb, and inferior maxillary atresia with glossoptosis. Also, carbon monoxide exposure between days 35 and 40 of embryonic development can lead to an increased risk of the child developing a cleft palate. Exposure to carbon monoxide or polluted ozone exposure can also lead to cardiac defects of the ventrical septal, pulmonary artery and heart valves.[37] The effects of carbon monoxide exposure are decreased later in fetal development during the fetal stage, but they may still lead to anoxic encephalopathy.[38]
Industrial pollution can also lead to congenital defects. Over a period of 37 years, the Chisso Corporation, a petrochemical and plastics company, contaminated the waters of Minamata Bay with an estimated 27 tons of methylmercury, contaminating the local water supply. This led to many people in the area developing what became known as the “Minamata Disease.” Because methylmercury is a teratogen, the mercury poisoning of those residing by the bay resulted in neurological defects in the offspring. Infants exposed to mercury poisoning in utero showed predispositions to cerebral palsy, ataxia, inhibited psychomotor development, and mental retardation.[39]
Landfill sites have been shown to have adverse effects on fetal development. Extensive research has been shown that landfills have several negative effects on babies born to mothers living near landfill sites: low birth weight, birth defects, spontaneous abortion, and fetal and infant mortality. Studies done around the Love Canal site near Niagara Falls and the Lipari Landfill in New Jersey have shown a higher proportion of low birth babies than communities farther away from landfills. A study done in California showed a positive correlation between time and quantity of dumping and low birth weights and neonatal deaths. A study in the United Kingdom showed a correspondence between pregnant women living near landfill sites and an increased risk of congenital disorders, such as neural tube defects, hypospadias, epispadia, and abdominal wall defects, such as gastroschisis and exomphalos. A study conducted on a Welsh community also showed an increase incidence of gastroschisis. Another study was done on twenty-one European hazardous waste sites and showed that those living within three kilometers had an increased risk of giving birth to infants with birth defects and that as distance from the land increased, the risk decreased. These birth defects included neural tube defects, malformations of the cardiac septa, anomalies of arteries and veins, and chromosomal anomalies.[40] Looking at communities that live near landfill sites brings up environmental justice. A vast majority of sites are located near poor, mostly black, communities. For example, between the early 1920s and 1978, about 25% of Houston’s population was black. However, over 80% of landfills and incinerators during this time were located in these black communities.[41]
Another issue regarding environmental justice is lead poisoning. If the fetus is exposed to lead during the pregnancy, this can result in learning difficulties and slowed growth. A lot of paints (before 1978) and pipes contain lead. Therefore, pregnant women who live in homes with lead paint will inhale the dust containing lead, leading to lead exposure in the fetus. When lead pipes are used for drinking water and cooking water, this water is ingested, along with the lead, exposing the fetus to this toxin. This issue is more prevalent in poorer communities. This is because more well off families are able to afford to have their homes repainted and pipes renovated.[42]
Paternal smoking
Paternal smoking prior to conception has been linked with the increased risk of congenital abnormalities in offspring.[5]
Smoking causes DNA mutations in the germ line of the father, which can be inherited by the offspring. Cigarette smoke acts as a chemical mutagen on germ cell DNA. The germ cells suffer oxidative damage, and the effects can be seen in altered mRNA production, infertility issues, and side effects in the embryonic and fetal stages of development. This oxidative damage may result in epigenetic or genetic modifications of the father's germ line. Research has shown that fetal lymphocytes have been damaged as a result of a father's smoking habits prior to conception.[7][26]
Correlations between paternal smoking and the increased risk of offspring developing childhood cancers (including acute leukemia, brain tumors, and lymphoma) before age five have been established. However, further research is needed to confirm these findings. Little is currently known about how paternal smoking damages the fetus, and what window of time in which the father smokes is most harmful to offspring.[26]
Infections
Main article: Vertically transmitted infection
A vertically transmitted infection is an infection caused by bacteria, viruses or, in rare cases, parasites transmitted directly from the mother to an embryo, fetus or baby during pregnancy or childbirth. It can occur when the mother gets an infection as an intercurrent disease in pregnancy.
Congenital disorders were initially believed to be the result of only hereditary factors. However, in the early 1940s, Australian pediatric ophthalmologist Norman Gregg began recognizing a pattern in which the infants arriving at his surgery were developing congenital cataracts at a higher rate than those who developed it from hereditary factors. On October 15, 1941, Gregg delivered a paper which explained his findings-68 out of the 78 children who were afflicted with congenital cataracts had been exposed in utero due to an outbreak in Australian army camps. These findings confirmed, to Gregg, that there could, in fact, be environmental causes for congenital disorders.
Currently rubella is known to cause abnormalities of the eye, internal ear, heart, and sometimes the teeth. More specifically, fetal exposure to rubella during weeks five to ten of development (the sixth week particularly) can cause cataracts and microphthalmia in the eyes. If the mother is infected with rubella during the ninth week, a crucial week for internal ear development, there can be destruction of the organ of Corti, causing deafness. In the heart the ductus arteriosus can remain after birth, leading to hypertension. Rubella can also lead to atrial and ventricular septal defects in the heart. If exposed to rubella in the second trimester, the fetus can develop central nervous system malformations. However, because infections of rubella may remain undetected,misdiagnosed, or unrecognized in the mother, and/or some abnormalities are not evident until later in the child’s life, precise incidence of birth defects due to rubella are not entirely known. The timing of the mother’s infection during fetal development determines the risk and type of birth defect. As the embryo develops, the risk of abnormalities decreases. If exposed to the rubella virus during the first four weeks, the risk of malformations is 47 percent. Exposure during weeks five through eight creates a 22 percent chance, while weeks nine to twelve a seven percent chance exists, followed by a percentage of six if the exposure is during the thirteenth to sixteenth weeks. Exposure during the first eight weeks of development can also lead to prematurity and fetal death. These numbers are calculated from immediate inspection of the infant after birth. Therefore, mental defects are not accounted for in the percentages because they are not evident until later in the child’s life. If they were to be included, these numbers would be much higher.[43]
Other infectious agents include cytomegalovirus, the herpes simplex virus, hyperthermia, toxoplasmosis, and syphilis. Mother exposure to cytomegalovirus can cause microcephaly, cerebral calcifications, blindess, chorioretinitis (which can cause blindness), hepatosplenomegaly, and meningoencephalitis in fetuses.[43] Microcephaly is a disorder in which the fetus has an atypically small head,[44] cerebral calcifications means certain areas of the brain have atypical calcium deposits,[45] and meningoencephalitis is the enlargement of the brain. All three disorders cause abnormal brain function or mental retardation. Hepatosplenomegaly is the enlargement of the liver and spleen which causes digestive problems.[46] It can also cause some kernicterus and petechiae. Kernicterus causes yellow pigmentation of the skin, brain damage, and deafness.[47] Petechaie is when the capillaries bleed resulting in red/purple spots on the skin.[48] However, cytomegalovirus is often fatal in the embryo.
The herpes simplex virus can cause microcephaly, microphthalmus (abnormally small eyeballs),[49] retinal dysplasia, hepatosplenomegaly, and mental retardation.[43] Both microphthalmus and retinal dysplasia can cause blindness. However, the most common symptom in infants is an inflammatory response that develops during the first three weeks of life.[43] Hyperthermia causes anencephaly, which is when part of the brain and skull are absent in the infant.[43][50] Mother exposure to toxoplasmosis can cause cerebral calcification, hydrocephalus (causes mental disabilities),[51] and mental retardation in infants. Other birth abnormalities have been reported as well, such as chorioretinitis, microphthalmus, and ocular defects. Syphilis causes congenital deafness, mental retardation, and diffuse fibrosis in organs, such as the liver and lungs, if the embryo is exposed.[43]
Lack of nutrients
Further information: Nutrition in pregnancy
For example, a lack of folic acid, a vitamin B, in the diet of a mother can cause cellular neural tube deformities that result in spina bifida. Congenital disorders such as a neural tube deformity (NTD) can be prevented by 72% if the mother consumes 4 milligrams of folic acid before the conception and after 12 weeks of pregnancy.[52] Folic acid, or vitamin B12, aids the development of the foetal nervous system.[52]
Studies with mice have found that food deprivation of the male mouse prior to conception leads to the offspring displaying significantly lower blood glucose levels.[53]
Physical restraint
External physical shocks or constrainment due to growth in a restricted space, may result in unintended deformation or separation of cellular structures resulting in an abnormal final shape or damaged structures unable to function as expected. An example is Potter syndrome due to oligohydramnios. This finding is important for future understandings of how genetics may predispose individuals for diseases like obesity, diabetes, and cancer.
For multicellular organisms that develop in a womb, the physical interference or presence of other similarly developing organisms such as twins can result in the two cellular masses being integrated into a larger whole, with the combined cells attempting to continue to develop in a manner that satisfies the intended growth patterns of both cell masses. The two cellular masses can compete with each other, and may either duplicate or merge various structures. This results in conditions such as conjoined twins, and the resulting merged organism may die at birth when it must leave the life-sustaining environment of the womb and must attempt to sustain its biological processes independently.
Genetic causes
Main article: Genetic disorder
Genetic causes of congenital anomalies include inheritance of abnormal genes from the mother or the father, as well as new mutations in one of the germ cells that gave rise to the fetus. Male germ cells mutate at a much faster rate than female germ cells, and as the father ages, the DNA of the germ cells mutates quickly.[6][25] If an egg is fertilized with sperm that has damaged DNA, there is a possibility that the fetus could develop abnormally.[6][22]
Genetic disorders or diseases are all congenital, though they may not be expressed or recognized until later in life. Genetic diseases may be divided into single-gene defects, multiple-gene disorders, or chromosomal defects. Single-gene defects may arise from abnormalities of both copies of an autosomal gene (a recessive disorder) or of only one of the two copies (a dominant disorder). Some conditions result from deletions or abnormalities of a few genes located contiguously on a chromosome. Chromosomal disorders involve the loss or duplication of larger portions of a chromosome (or an entire chromosome) containing hundreds of genes. Large chromosomal abnormalities always produce effects on many different body parts and organ systems.
Socioeconomic status
A low socioeconomic status in a deprived neighborhood may include exposure to “environmental stressors and risk factors.”[54] Socioeconomic inequalities are commonly measured by the Cartairs-Morris score, Index of Multiple Deprivation, Townsend deprivation index, and the Jarman score.[55] The Jarman score, for example, considers “unemployment, overcrowding, single parents, under-fives, elderly living alone, ethnicity, low social class and residential mobility.”[55] In Vos’ meta-analysis these indices are used to view the effect of low SES neighborhoods on maternal health. In the meta-analysis, data from individual studies were collected from 1985 up until 2008.[55] Vos concludes that a correlation exists between prenatal adversities and deprived neighborhoods.[55] Other studies have shown that low SES is closely associated with the development of the fetus in utero and growth retardation.[56] Studies also suggest that children born in low SES families are “likely to be born prematurely, at low birth weight, or with asphyxia, a birth defect, a disability, fetal alcohol syndrome, or AIDS.”[56] Bradley and Corwyn also suggest that congenital disorders arise from the mother’s lack of nutrition, a poor lifestyle, maternal substance abuse and “living in a neighborhood that contains hazards affecting fetal development (toxic waste dumps).”[56] In a meta-analysis that viewed how inequalities influenced maternal health, it was suggested that deprived neighborhoods often promoted behaviors such as smoking, drug and alcohol use.[54] After controlling for socioeconomic factors and ethnicity, several individual studies demonstrated an association with outcomes such as perinatal mortality and preterm birth.[54]
Role of radiation
For the survivors of the atomic bombing of Hiroshima and Nagasaki, who are known as the Hibakusha, no statistically demonstrable increase of birth defects/congenital malformations was found among their later conceived children, or found in the later conceived children of cancer survivors who had previously received radiotherapy.[57][58][59] [60] The surviving women of Hiroshima and Nagasaki who were able to conceive, though exposed to substantial amounts of radiation, later had children with no higher incidence of abnormalities/birth defects than in the Japanese population as a whole.[61][62]
Relatively few studies have researched the effects of paternal radiation exposure on offspring. Following the Chernobyl disaster, it was found that the germ line of irradiated fathers suffered minisatellite mutations in the DNA, which was inherited by descendants.[21][63] Animal studies have show that the X-ray irradiation of male mice resulted in birth defects of the offspring.[7]
In the 1980s, a relatively high prevalence of pediatric leukemia cases in children living near a nuclear processing plant in West Cumbria, UK, led researchers to investigate whether the cancer was a result of paternal radiation exposure. A significant association between paternal irradiation and offspring cancer was found, but further research areas close to other nuclear processing plants did not produce the same results.[7][21]
Father's age
Main article: Paternal age effect
The effects of paternal age on offspring are not yet well understood and are studied far less extensively than the effects of maternal age.[64] Fathers contribute proportionally more DNA mutations to their offspring via their germ cells than the mother, with the paternal age governing how many mutations are passed on. This is because, as humans age, male germ cells acquire mutations at a much faster rate than female germ cells.[6][7][25]
Around a 5% increase in the incidence of ventricular septal defects, atrial septal defects, and patent ductus arteriosus in offspring has been found to be correlated with advanced paternal age. Advanced paternal age has also been linked to increased risk of achondroplasia and Apert syndrome. Offspring born to fathers under the age of 20 show increased risk of being affected by patent ductus arteriosus, ventricular septal defects, and the tetralogy of Fallot. It is hypothesized that this may be due to environmental exposures or lifestyle choices.[64]
Research has found that there is a correlation between advanced paternal age and risk of birth defects such as limb anomalies, syndromes involving multiple systems, and Down's syndrome.[6][25][65] Recent studies have concluded that 5-9% of Down's syndrome cases are due to paternal effects, but these findings are controversial.[6][22][25][66]
There is concrete evidence that advanced paternal age is associated with the increased likelihood that a mother will suffer from a miscarriage or that fetal death will occur.[6]
Unknown or multifactorial
Although significant progress has been made in identifying the etiology of some birth defects, approximately 65% have no known or identifiable cause.[24] These are referred to as sporadic, a term that implies an unknown cause, random occurrence regardless of maternal living conditions,[67] and a low recurrence risk for future children. For 20-25% of anomalies there seems to be a "multifactorial" cause, meaning a complex interaction of multiple minor genetic anomalies with environmental risk factors. Another 10-13% of anomalies have a purely environmental cause (e.g. infections, illness, or drug abuse in the mother). Only 12-25% of anomalies have a purely genetic cause. Of these, the majority are chromosomal anomalies.[68]
Epidemiology
Disability-adjusted life year for congenital anomalies per 100,000 inhabitants in 2004.[69]
no data
less than 160
160-240
240-320
320-400
400-480
480-560
560-640
640-720
720-800
800-900
900-950
more than 950
Congenital anomalies resulted in about 632,000 deaths per year in 2013 down from 751,000 in 1990.[9] The type with the greatest death are congenital heart disease (323,000), followed by neural tube defects (69,000).[9]
Many studies have found that the frequency of occurrence of certain congenital malformations depends on the sex of the child (table).[70][71][72][73][74] For example, pyloric stenosis occurs more often in males while congenital hip dislocation is four to five times more likely to occur in females. Among children with one kidney, there are approximately twice as many males, whereas among children with three kidneys there are approximately 2.5 times more females. The same pattern is observed among infants with excessive number of ribs, vertebrae, teeth and other organs which in a process of evolution have undergone reduction—among them there are more females. Contrarily, among the infants with their scarcity, there are more males. Anencephaly is shown to occur approximately twice as frequently in females.[75] The number of boys born with 6 fingers is two times higher than the number of girls.[76] Now various techniques are available to detect congenital anomalies in fetus before birth.[citation needed]
About 3% of newborns have a "major physical anomaly", meaning a physical anomaly that has cosmetic or functional significance.[77] Physical congenital abnormalities are the leading cause of infant mortality in the United States, accounting for more than 20% of all infant deaths. Seven to ten percent of all children[clarification needed] will require extensive medical care to diagnose or treat a birth defect.[78]
-
The sex ratio of patients with congenital malformations
| Congenital anomaly |
Sex ratio, ♂♂:♀♀ |
| Defects with female predominance |
|
| Congenital hip dislocation |
1 : 5.2;[79] 1 : 5;[80] 1 : 8;[74] 1 : 3.7[81] |
| Cleft palate |
1 : 3[80] |
| Anencephaly |
1 : 1.9;[79] 1 : 2[75] |
| Craniocele |
1 : 1.8[79] |
| Aplasia of lung |
1 : 1.51[79] |
| Spinal herniation |
1 : 1.4[79] |
| Diverticulum of the esophagus |
1 : 1.4[79] |
| Stomach |
1 : 1.4[79] |
| Neutral defects |
|
| Hypoplasia of the tibia and femur |
1 : 1.2[79] |
| Spina bifida |
1 : 1.2[81] |
| Atresia of small intestine |
1 : 1[79] |
| Microcephaly |
1.2 : 1[81] |
| Esophageal atresia |
1.3 : 1;[79] 1.5 : 1[81] |
| Hydrocephalus |
1.3 : 1[81] |
| Defects with male predominance |
|
| Diverticula of the colon |
1.5 : 1[79] |
| Atresia of the rectum |
1.5 : 1;[79] 2 : 1[81] |
| Unilateral renal agenesis |
2 : 1;[79] 2.1 : 1[81] |
| Schistocystis |
2 : 1[79] |
| Cleft lip and palate |
2 : 1;[80] 1.47 : 1[81] |
| Bilateral renal agenesis |
2.6 : 1[79] |
| Congenital anomalies of the genitourinary system |
2.7 : 1[74] |
| Pyloric stenosis, congenital |
5 : 1;[80] 5.4 : 1[74] |
| Meckel's diverticulum |
More common in boys[79] |
| Congenital megacolon |
More common in boys[79] |
| All defects |
1.22 : 1;[82] 1.29 : 1[74] |
- Data[74] obtained on opposite-sex twins. ** — Data[81] were obtained in the period 1983-1994.
P. M. Rajewski and A. L. Sherman (1976) have analyzed the frequency of congenital anomalies in relation to the system of the organism. Prevalence of men was recorded for the anomalies of phylogenetically younger organs and systems.[79]
In respect of an etiology, sexual distinctions can be divided on appearing before and after differentiation of male's gonads in during embryonic development, which begins from eighteenth week. The testosterone level in male embryos thus raises considerably.[83] The subsequent hormonal and physiological distinctions of male and female embryos can explain some sexual differences in frequency of congenital defects. It is difficult to explain the observed differences in the frequency of birth defects between the sexes by the details of the reproductive functions or the influence of environmental and social factors.
United States
The CDC and National Birth Defect Project studied the incidence of birth defects in the US. Key findings include:
- Down syndrome was the most common condition with an estimated prevalence of 14.47 per 10,000 live births, implying about 6,000 diagnoses each year.
- About 7,000 babies are born with a cleft palate, cleft lip or both.
Adjusted National Prevalence Estimates and Estimated Number of Cases in the United States, 2004-2006[84]
| Birth Defects |
Cases per Births |
Estimated Annual Number of Cases |
Estimated National Prevalence per 10,000 Live Births (Adjusted for maternal race/ethnicity) |
| Central nervous system defects |
| Anencephaly |
1 in 4,859 |
859 |
2.06 |
| Spina bifida without anencephaly |
1 in 2,858 |
1460 |
3.50 |
| Encephalocele |
1 in 12,235 |
341 |
0.82 |
| Eye defects |
| Anophthalmia/ microphthalmia |
1 in 5,349 |
780 |
1.87 |
| Cardiovascular defects |
| Common truncus |
1 in 13,876 |
301 |
0.72 |
| Transposition of great arteries |
1 in 3,333 |
1252 |
3.00 |
| Tetralogy of Fallot |
1 in 2,518 |
1657 |
3.97 |
|
| Atrioventricular septal defect |
1 in 2,122 |
1966 |
4.71 |
| Hypoplastic left heart syndrome |
1 in 4,344 |
960 |
2.30 |
| Orofacial defects |
| Cleft palate without cleft lip |
1 in 1,574 |
2651 |
6.35 |
| Cleft lip with and without cleft palate |
1 in 940 |
4437 |
10.63 |
| Gastrointestinal defects |
| Esophageal atresia/tracheoeophageal fistula |
1 in 4,608 |
905 |
2.17 |
| Rectal and large intestinalatresia/stenosis |
1 in 2,138 |
1952 |
4.68 |
| Musculoskeletal defects |
| Reduction deformity, upper limbs |
1 in 2,869 |
1454 |
3.49 |
| Reduction deformity, lower limbs |
1 in 5,949 |
701 |
1.68 |
| Gastroschisis |
1 in 2,229 |
1871 |
4.49 |
| Omphalocele |
1 in 5,386 |
775 |
1.86 |
| Diaphragmatic hernia |
1 in 3,836 |
1088 |
2.61 |
| Chromosomal anomalies |
| Trisomy 13 |
1 in 7,906 |
528 |
1.26 |
| Trisomy 21 (Down syndrome) |
1 in 691 |
6037 |
14.47 |
| Trisomy 18 |
1 in 3,762 |
1109 |
2.66 |
See also
- Malformative syndrome
- ICD-10 Chapter Q: Congenital malformations, deformations and chromosomal abnormalities
- Idiopathic
- List of congenital disorders
- List of ICD-9 codes 740-759: Congenital anomalies
- March of Dimes
- Mitochondrial disease
- Supernumerary body part
References
Wikipedia and research
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External links
- CDC’s National Center on Birth Defects and Developmental Disabilities
- Birth Defect Research for Children
|
Chromosome abnormalities (Q90–Q99, 758)
|
|
| Autosomal |
| Trisomies |
- Down syndrome
- Edwards syndrome
- Patau syndrome
- Trisomy 9
- Warkany syndrome 2
- Cat eye syndrome/Trisomy 22
- Trisomy 16
|
|
| Monosomies/deletions |
- 1q21.1 deletion syndrome/1q21.1 duplication syndrome/TAR syndrome
- Wolf–Hirschhorn syndrome
- Cri du chat/Chromosome 5q deletion syndrome
- Williams syndrome
- Jacobsen syndrome
- Miller–Dieker syndrome/Smith–Magenis syndrome
- DiGeorge syndrome
- 22q11.2 distal deletion syndrome
- 22q13 deletion syndrome
- genomic imprinting
- Angelman syndrome/Prader–Willi syndrome (15)
- Distal 18q-/Proximal 18q-
|
|
|
| X/Y linked |
| Monosomy |
|
|
Trisomy/tetrasomy,
other karyotypes/mosaics |
- Klinefelter syndrome (47,XXY)
- 48,XXYY
- 48,XXXY
- 49,XXXYY
- 49,XXXXY
- Triple X syndrome (47,XXX)
- 48,XXXX
- 49,XXXXX
|
|
|
| Translocations |
| Leukemia/lymphoma |
| Lymphoid |
- Burkitt's lymphoma t(8 MYC;14 IGH)
- Follicular lymphoma t(14 IGH;18 BCL2)
- Mantle cell lymphoma/Multiple myeloma t(11 CCND1:14 IGH)
- Anaplastic large-cell lymphoma t(2 ALK;5 NPM1)
- Acute lymphoblastic leukemia
|
|
| Myeloid |
- Philadelphia chromosome t(9 ABL; 22 BCR)
- Acute myeloblastic leukemia with maturation t(8 RUNX1T1;21 RUNX1)
- Acute promyelocytic leukemia t(15 PML,17 RARA)
- Acute megakaryoblastic leukemia t(1 RBM15;22 MKL1)
|
|
|
| Other |
- Ewing's sarcoma t(11 FLI1; 22 EWS)
- Synovial sarcoma t(x SYT;18 SSX)
- Dermatofibrosarcoma protuberans t(17 COL1A1;22 PDGFB)
- Myxoid liposarcoma t(12 DDIT3; 16 FUS)
- Desmoplastic small-round-cell tumor t(11 WT1; 22 EWS)
- Alveolar rhabdomyosarcoma t(2 PAX3; 13 FOXO1) t (1 PAX7; 13 FOXO1)
|
|
|
| Other |
- Fragile X syndrome
- Uniparental disomy
- XX male syndrome
- Ring chromosome (13; 14; 15; 20)
|
|
