micrencephaly

小脳髄症

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/10/18 17:49:31」(JST)

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"Microcephalus" redirects here. For the genus of beetle, see Microcephalus (genus).

Microcephaly
A baby with microcephaly (left) compared to a baby with a typical head size
Classification and external resources
Specialty	Medical genetics
ICD-10	Q02
ICD-9-CM	742.1
OMIM	251200
DiseasesDB	22629
MedlinePlus	003272
MeSH	D008831

Microcephaly is a medical condition in which the brain does not develop properly resulting in a smaller than normal head. Microcephaly may be present at birth or it may develop in the first few years of life. Often people with the disorder have an intellectual disability, poor motor function, poor speech, abnormal facial features, seizures, and dwarfism.

The disorder may stem from a wide variety of conditions that cause abnormal growth of the brain, or from syndromes associated with chromosomal abnormalities. A homozygous mutation in one of the microcephalin genes causes primary microcephaly. It serves as an important neurological indication or warning sign, but no uniformity exists in its definition. It is usually defined as a head circumference (HC) more than two standard deviations below the mean for age and sex. Some academics advocate defining it as head circumference more than three standard deviations below the mean for the age and sex.

There is no specific treatment that returns the head size to normal. In general, life expectancy for individuals with microcephaly is reduced and the prognosis for normal brain function is poor. Occasionally, some will grow normally and develop normal intelligence.

Signs and symptoms

Affected newborns generally have striking neurological defects and seizures. Severely impaired intellectual development is common, but disturbances in motor functions may not appear until later in life.

Infants with microcephaly are born with either a normal or reduced head size. Subsequently, the head fails to grow, while the face continues to develop at a normal rate, producing a child with a small head and a receding forehead, and a loose, often wrinkled scalp. As the child grows older, the smallness of the skull becomes more obvious, although the entire body also is often underweight and dwarfed. Development of motor functions and speech may be delayed. Hyperactivity and intellectual disability are common occurrences, although the degree of each varies. Convulsions may also occur. Motor ability varies, ranging from clumsiness in some to spastic quadriplegia in others.

Causes

Neural scans of a normal-sized skull (left) and a case of microcephaly (right)

Microcephaly is a type of cephalic disorder. It has been classified in two types based on the onset:

Congenital

Isolated

1. Familial (autosomal recessive) microcephaly
2. Autosomal dominant microcephaly
3. X-linked microcephaly
4. Chromosomal (balanced rearrangements and ring chromosome)

Syndromes

• Chromosomal

1. Poland syndrome
2. Down syndrome
3. Edward syndrome
4. Patau syndrome
5. Unbalanced rearrangements

• Contiguous gene deletion

1. 4p deletion (Wolf–Hirschhorn syndrome)
2. 5p deletion (Cri-du-chat)
3. 7q11.23 deletion (Williams syndrome)
4. 22q11 deletion (DiGeorge syndrome)

• Single gene defects

1. Smith–Lemli–Opitz syndrome
2. Seckel syndrome
3. Cornelia de Lange syndrome
4. Holoprosencephaly
5. Primary microcephaly 4

Acquired

• Disruptive injuries

1. Ischemic stroke
2. Hemorrhagic stroke
3. Death of a monozygotic twin

• Vertically transmitted infections

1. Congenital cytomegalovirus infection
2. Toxoplasmosis
3. Congenital rubella syndrome
4. Zika virus

• Drugs

1. Fetal hydantoin syndrome
2. Fetal alcohol syndrome

Other

1. Radiation exposure to mother
2. Maternal malnutrition
3. Maternal phenylketonuria
4. Poorly controlled gestational diabetes
5. Hyperthermia
6. Maternal hypothyroidism
7. Placental insufficiency

Postnatal onset

Genetic

• Inborn errors of metabolism

1. Congenital disorder of glycosylation
2. Mitochondrial disorders
3. Peroxisomal disorder
4. Glucose transporter defect
5. Menkes disease
6. Congenital disorders of amino acid metabolism
7. Organic acidemia

Syndromes

• Contiguous gene deletion

1. 17p13.3 deletion (Miller–Dieker syndrome)

• Single gene defects

1. Rett syndrome (primarily girls)
2. Nijmegen breakage syndrome
3. X-linked lissencephaly with abnormal genitalia
4. Aicardi–Goutières syndrome
5. Ataxia telangiectasia
6. Cohen syndrome
7. Cockayne syndrome

Acquired

• Disruptive injuries

1. Traumatic brain injury
2. Hypoxic-ischemic encephalopathy
3. Ischemic stroke
4. Hemorrhagic stroke

• Infections

1. Congenital HIV encephalopathy
2. Meningitis
3. Encephalitis

• Toxins

1. Lead poisoning
2. Chronic renal failure

• Deprivation

1. Hypothyroidism
2. Anemia
3. Congenital heart disease
4. Malnutrition

Genetic factors may play a role in causing some cases of microcephaly. Relationships have been found between autism, duplications of chromosomes, and macrocephaly on one side. On the other side, a relationship has been found between schizophrenia, deletions of chromosomes, and microcephaly. Moreover, an association has been established between common genetic variants within known microcephaly genes (MCPH1, CDK5RAP2) and normal variation in brain structure as measured with magnetic resonance imaging (MRI)‍—‌i.e., primarily brain cortical surface area and total brain volume.

The spread of Aedes mosquito-borne Zika virus has been implicated in increasing levels of congenital microcephaly by the International Society for Infectious Diseases and the US Centers for Disease Control and Prevention. Zika can spread from a pregnant woman to her fetus. This can result in other severe brain malformations and birth defects. A study published in The New England Journal of Medicine has documented a case in which they found evidence of the Zika virus in the brain of a fetus that displayed the morphology of microcephaly.

Microencephaly

"Microcephaly" means "smallheadedness" (New Latin microcephalia, from Ancient Greek μικρός mikrós "small" and κεφαλή kephalé "head"). "Microencephaly" means "small brain". Because the size of the brain is mostly determined by the size of the head, microencephaly is implied when discussing microcephaly.

Other

After the dropping of atomic bombs "Little Boy" on Hiroshima and "Fat Man" on Nagasaki, several women close to ground zero who had been pregnant at the time gave birth to children with microcephaly. Microcephaly prevalence was seven of a group of 11 pregnant women at 11–17 weeks of gestation who survived the blast at less than 1.2 km (0.75 mi) from ground zero. Due to their proximity to the bomb, the pregnant women's in utero children received a biologically significant radiation dose that was relatively high due to the massive neutron output of the lower explosive-yielding Little Boy. Microcephaly is the only proven malformation, or congenital abnormality, found in the children of Hiroshima and Nagasaki.

Pathophysiology

Microcephaly generally is due to the diminished size of the largest part of the human brain, the cerebral cortex, and the condition can arise during embryonic and fetal development due to insufficient neural stem cell proliferation, impaired or premature neurogenesis, the death of neural stem cells or neurons, or a combination of these factors. Research in animal models such as rodents has found many genes that are required for normal brain growth. For example the Notch pathway genes regulate the balance between stem cell proliferation and neurogenesis in the stem cell layer known as the ventricular zone, and experimental mutations of many genes can cause microcephaly in mice, similar to human microcephaly. In addition, viruses such as cytomegalovirus (CMV) or Zika have been shown to infect and kill the primary stem cell of the brain—the radial glial cell, resulting in the loss of future daughter neurons. The severity of the condition may depend on the timing of infection during pregnancy.

Treatment

Baby with microcephaly during a physical therapy session

There is no known cure for microcephaly. Treatment is symptomatic and supportive.

History

People with microcephaly were sometimes sold to freak shows in North America and Europe in the 19th and early 20th centuries, where they were known by the name "pinheads". Many of them were presented as different species (e.g., "monkey man") and described as being the missing link. Famous examples are Zip the Pinhead (although he may not have had microcephaly) and Schlitzie the Pinhead, who also starred in the 1932 movie Freaks. Both these individuals were cited as influences on the development of the long-running comic strip character Zippy the Pinhead, created by Bill Griffith.

Notable cases

• Triboulet was a jester of duke René of Anjou (not to be confused with the slightly later Triboulet at the French court).
• Jenny Lee Snow and Elvira Snow, commonly referred to as Pip and Flip, were sisters with microcephaly who acted in the 1932 film Freaks.
• Schlitze "Schlitzie" Surtees, possibly born Simon Metz, was a sideshow performer and actor.
• Lester "Beetlejuice" Napoleon Green, known on the Howard Stern Show for being "The Greatest Wack Packer of All Time"

See also

• Anencephaly (Usually rapidly fatal)
• Hydrocephaly
• Macrocephaly
• Seckel syndrome

References

External links

• Microcephaly at NINDS
• Microcephaly Support Group
• The Rat People of Pakistan
• NINDS Overview
• Schlitzie The Pinhead
• Head circumference percentile calculator

UpToDate Contents

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• 1. 幼児および小児における小頭症：病因および評価 microcephaly in infants and children etiology and evaluation

English Journal

• Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization.

• Chen CP, Lin CJ, Chang TY, Chern SR, Wu PS, Chen YT, Su JW, Lee CC, Chen LF, Wang W.SourceDepartment of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan; Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan; Department of Medicine, Mackay Medical College, New Taipei City, Taiwan; Department of Biotechnology, Asia University, Taichung, Taiwan; School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan; Institute of Clinical and Community Health Nursing, National Yang-Ming University, Taipei, Taiwan; Department of Obstetrics and Gynecology, School of Medicine, National Yang-Ming University, Taipei, Taiwan. Electronic address: cpc_mmh@yahoo.com.
• Gene.Gene.2013 Apr 25;519(1):164-168. doi: 10.1016/j.gene.2013.01.055. Epub 2013 Feb 9.
• We present rapid aneuploidy diagnosis of ring chromosome 2 with 2p25.3 and 2q37.3 microdeletions by aCGH using uncultured amniocytes in a fetus with IUGR, microcephaly, lissencephaly and ambiguous external genitalia. Our case adds lissencephaly to the list of CNS abnormalities in ring chromosome 2 w
• PMID 23403238

• Germline mosaicism in Rubinstein-Taybi syndrome.

• Tajir M, Fergelot P, Lancelot G, Elalaoui SC, Arveiler B, Lacombe D, Sefiani A.SourceCentre de Génomique Humaine, Faculté de Médecine et de Pharmacie, Université Mohamed V Souissi, Rabat, Maroc; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Maroc. Electronic address: mariam_tajir@yahoo.fr.
• Gene.Gene.2013 Apr 15;518(2):476-8. doi: 10.1016/j.gene.2012.12.105. Epub 2013 Jan 23.
• Rubinstein-Taybi syndrome is an autosomal dominant disorder with multiple congenital anomalies and genetic heterogeneity. Clinical manifestations include mental retardation, postnatal growth deficiency, microcephaly, broad thumbs and halluces, and characteristic facial features. Mutations in the gen
• PMID 23352794

• ATR localizes to the photoreceptor connecting cilium and deficiency leads to severe photoreceptor degeneration in mice.

• Valdés-Sánchez L, De la Cerda B, Diaz-Corrales FJ, Massalini S, Chakarova CF, Wright AF, Bhattacharya SS.SourceThe authors wish to be known that, in their opinion, the first three authors should be regarded as joint first authors.
• Human molecular genetics.Hum Mol Genet.2013 Apr 15;22(8):1507-15. doi: 10.1093/hmg/dds563. Epub 2013 Jan 7.
• Ataxia-telangiectasia and Rad3 (ATR), a sensor of DNA damage, is associated with the regulation and control of cell division. ATR deficit is known to cause Seckel syndrome, characterized by severe proportionate short stature and microcephaly. We used a mouse model for Seckel disease to study the eff
• PMID 23297361

Japanese Journal

• Dose-response relationship of N-methyl-N-nitrosourea in inducing micrencephaly in mouse off-spring (NEREVOUS SYSTEM) (GENERAL SESSION BY POSTER PRESENTATION) (Proceedings of the 30th Annual Meeting)

• KOBAYASHI HARUO,NODA HIROFUMI,HOSSAIN MUHAMMAD,SUZUKI TADAHIKO,SATO ITARU,SUZUKI KOICHI
• Journal of toxicological sciences 28(4), 316, 2003-10-31
• NAID 110001812746

• The central nervous system in microcephalic primordial dwarfism : Is there a characteristic developmental brain pathology in Seckel or Seckel-like syndrome?

• Schmitt Horst P.,Sergi Consolato
• Congenital anomalies 40(1), 32-39, 2000-03
• NAID 110002785620

Related Links

• Micrencephaly | Define Micrencephaly at Dictionary.com

micrencephaly mi·cren·ceph·a·ly (mī'krěn-sěf'ə-lē) or mi·cro·en·ceph·a·ly (mī'krō-ěn-) n. The condition of having an abnormally small brain.

• micrencephaly - definition of micrencephaly by Medical dictionary

micrencephaly /mi·cren·ceph·a·ly/ (mi″kren-sef´ah-le) abnormal smallness of the brain.micrenceph´alous mi·cren·ceph·a·ly (mī′krĕn-sĕf′ə-lē) or mi·cro·en·ceph·a·ly (mī′krō-ĕn-) n. The condition of having an abnormally small brain.

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