| Fucosidosis |
| Classification and external resources |
|
Fucose
|
| ICD-10 |
E77.1 |
| ICD-9 |
271.8 |
| OMIM |
230000 |
| DiseasesDB |
29471 |
| MeSH |
D005645 |
Fucosidosis is a rare lysosomal storage disorder[1] in which the FUCA1 gene experiences mutations that severely reduce or stop the activity of the alpha-L-fucosidase enzyme.[2] The result is a buildup of complex sugars in parts of the body, which leads to death. Fucosidosis is one of nine identified glycoprotein storage diseases. The gene encoding the alpha-fucosidase, FUCA 1, was found to be located to the short arm of chromosome 1p36 - p34,[3] by Carrit and co-workers, in 1982.[4]
Contents
- 1 Disease
- 2 History
- 3 Type 1
- 4 Type 2
- 5 Type 3
- 6 Treatment
- 7 Diagnosis
- 8 Other forms
- 9 See also
- 10 External links
Disease
Fucosidosis is an autosomal recessive disorder that affects many areas of the body. Mutations in the FUCA1 gene causes fucosidosis. The FUCA1 gene provides instructions for making an enzyme called alpha-L-fucosidase. The enzyme plays a role in the breakdown of complex sugars in the body.[5] The disorder is characterized by lysosomal accumulation of a variety of glycoproteins, glycolipids, and oligosaccharides that contain fucose moieties.[6] The deficiency of the enzyme alpha-L-fucosidase, which is used to metabolize complex compounds in the body (fucose-containing glycolipids and fucose-containing glycoproteins). With the lack of this enzyme activity, the result is incomplete breakdown of glycolipids and glycoproteins. These partially broken down compounds accumulate in various parts of the body and begin to cause malfunction in cells.[7] Brain cells are especially sensitive to this buildup and can eventually cause cell death. Other results are progressive neurological deterioration, skin abnormalities, growth retardation, skeletal disease, and coarsening of facial features.[8] Fucosidosis is the consequence of faulty degradation of both sphingolipids and polysaccharides. Major accumulation of the H-antigen (a member of the ABO blood group antigens), a glycolipid, is seen primarily in the liver of fucosidosis patients.[9]
History
Fucosidosis is an extremely rare disorder first described in 1962 in two Italian siblings that showed progressive mental retardation and neurological deterioration. The disease itself is extremely rare (less than 100 documented cases[10]) only affecting 1:2,000,000[11] (with most cases being prevalent in Italy, Cuba, and the southwest U.S). The disease has three different types to it. Type 1 and 2 being considered severe and Type 3 being a mild disease.[12] Symptoms are highly variable with mild cases being able to live within the third or fourth decade. Type 1 and 2 are both linked with mental retardation. Severe cases can develop life-threatening complications early in childhood.[13] Because the major accumulating glycoconjugate in fucosidosis patients is the blood group H-antigen it is intriguing to speculate, but the evidence is not clear at this time, that blood type may affect the course of the disease.[14]
Type 1
Type 1 usually begins somewhere in the 10 months of age and in considered the most severe of the three types.[15] Symptoms include:
- Coarse facial features
- Enlarged liver, spleen, and/or heart
- Mental retardation
- Seizures
- Abnormal bone formation of many bones
- Progressive deterioration of brain and spinal cord
- Increased or decreased perspiration
Patients have no vascular lesions, but have rapid psychomotor regression, severe and rapidly progressing neurologic signs, elevated sodium and chloride excretion in the sweat, and fatal outcome before the sixth year.
Type 2
Type 2 appears in when a child is around 18 months of age and in considered milder than Type 1 but still severe.[16] Symptoms include:
- Symptoms similar to Type 1 but milder and progress more slowly.
- Horny or warty growth over blood vessels on the skin.
Type 3
Type 3 appears around 1–2 years of age and is considered mild[17]
Treatment
Treatment: No treatment or way to reverse. Treatment will focus on the symptoms an individual has, such as seizure medication.
- It is possible that if an individual receives a bone marrow transplant, they could receive healthy bone marrow cells which would product normal amounts of fucosidase. But there not enough info to prove this in an effective treatment.[18]
Diagnosis
Diagnosis: A special urine test is used to check for broken any partially broken-down-sugars. If they are present, a skin or blood sample will be taken. If skin or blood has below-normal amounts of alpha-fucosidase in it, you have fucosidosis.[19]
- Fucosidosis is an autosomal recessive disorder (Both copies of the gene in the must have the mutation). Both parents have to have the gene and pass it on to the child. There is a 25% chance of this being passed on.
Other forms
Canine fucosidosis is found in the English Springer Spaniel. The disease affects the ability to break down the enzyme alpha-fucosidase. The enzyme deficiency prohibits the breakdown and metabolism of complex polysaccharides from within cells.[20]
Typically affecting dogs between 18 months and four years, symptoms include:
- Loss of learned behavior
- Change in temperament
- Blindness
- Loss of balance
- Deafness
- Weight loss
- From the onset, disease progress is quick and fatal.
Just like the human version, canine fucosidosis is a recessive disorder and two copies of the gene must be present, one from each parent, in order to show symptoms of the disease.
References
- ^ http://www.horsetesting.com/Canine/Fucosidosis.htm
- ^ http://ghr.nlm.nih.gov/condition=fucosidosis
- ^ http://themedicalbiochemistrypage.org/fucosidosis.php
- ^ http://www.ismrd.org/the_diseases/fucosidosis/genetics_of_fucosidosis
- ^ http://ghr.nlm.nih.gov/condition/fucosidosis
- ^ http://themedicalbiochemistrypage.org/fucosidosis.php
- ^ http://ghr.nlm.nih.gov/condition=fucosidosis
- ^ http://children.webmd.com/fucosidosis - Children.webmd
- ^ http://themedicalbiochemistrypage.org/fucosidosis.php
- ^ http://themedicalbiochemistrypage.org/fucosidosis.php
- ^ http://www.ismrd.org/the_diseases/fucosidosis/genetics_of_fucosidosis
- ^ http://rarediseases.about.com/od/rarediseasesf/a/fucosidosis.htm
- ^ http://children.webmd.com/fucosidosis - Children.webmd
- ^ http://themedicalbiochemistrypage.org/fucosidosis.php
- ^ http://rarediseases.about.com/od/rarediseasesf/a/fucosidosis.htm
- ^ http://rarediseases.about.com/od/rarediseasesf/a/fucosidosis.htm
- ^ http://rarediseases.about.com/od/rarediseasesf/a/fucosidosis.htm
- ^ http://rarediseases.about.com/od/rarediseasesf/a/fucosidosis.htm
- ^ http://rarediseases.about.com/od/rarediseasesf/a/fucosidosis.htm
- ^ http://www.horsetesting.com/Canine/Fucosidosis.htm
See also
External links
- http://ghr.nlm.nih.gov/condition=fucosidosis
- http://www.ismrd.org/the_diseases/fucosidosis/genetics_of_fucosidosis
- http://www.rarediseases.org/rare-disease-information/rare-diseases/byID/1095/viewAbstract - Rare diseases.org
- http://rarediseases.about.com/od/rarediseasesf/a/fucosidosis.htm
- http://children.webmd.com/fucosidosis - Children.webmd
- http://www.horsetesting.com/Canine/Fucosidosis.htm
|
(LSD) Inborn error of carbohydrate metabolism: glycoproteinosis (E77, 271.8)
|
|
| Anabolism |
- Dolichol kinase deficiency
- Congenital disorder of glycosylation
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Post-translational modification
of lysosomal enzymes |
- Mucolipidosis: I-cell disease/II
- Pseudo-Hurler polydystrophy/III
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| Catabolism |
- Aspartylglucosaminuria
- Fucosidosis
- mannosidosis
- Alpha-mannosidosis
- Beta-mannosidosis
- Sialidosis
- Schindler disease
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| Other |
- solute carrier family (Salla disease)
- Galactosialidosis
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mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m
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k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon
|
m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)
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