Difference between revisions of "Metachromatic leukodistrophy"

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== Summary ==
 
Metachromatic leukodistrophy (MLD) is an incurable, autosomal recessive inherited disease, which is caused by a mutation in the enzyme Arylsulfatase A (ARS A) and belongs to the lysosomal storage diseases. In MLD, the activity of ARS A is usually less than 10 % of the normal activity. As ARS A normally breaks down sulfatides, such low activity leads to storage of sulfatides. The storage of the lipids glycosphingolipid sulfatide and lysosulfatide cause a degeneration of the white matter in the brain. This part of the brain mainly consists of myelinated axons, which are needed for the proper function of the brain. <ref name="blomqusit2011">Blomqvist, Maria. Gieselmann,Volkmar. Mansson,Jan-Eric. "Accumulation of lysosulfatide in the brain of arylsulfatase A-deficient mice". Lipids in Health and Disease, 2011</ref>
 
Five different allelic and two non-allelic variants of the disease have been characterized.
 
 
== Phenotype ==
 
Five different allelic variants have been described. Depending on the variant, onset and type of symptoms and progression of the disease can be different (QUELLE: OMIM, Wikipedia):
 
 
* '''Late infantile''': Carriers of the disease causing alleles usually become diseased two years after birth. The patients show motor symptoms, rigidity, mental deterioration, and sometimes convulsions. Death occurs five years after breakout of the disease at the latest (example study: [http://www.ncbi.nlm.nih.gov/pubmed/5963214]).(OMIM+wikipedia)
 
* '''Juvenile''': Onset is between 3–10 years of age. The disease usually begins with impaired school performance, mental deterioration and dementia. Then, symptoms strongly resemble the late infantile form. As the progression is slower than in the juvenile form, patients normally die 10 to 15 years after the start of the symptoms (example study: [http://www.ncbi.nlm.nih.gov/pubmed/5963214]). (OMIM+wikipedia)
 
* '''Adult forms''': This form of MLD begins after the age of 16. Symptoms are commonly psychiatric and can lead to the diagnosis of schizophrenia. Disorders in movement and posture appear very late. The progression of the disease is even slower than in the "late infantile" and "juvenile" forms and patients may live for another several decades after onset of the symptoms. (OMIM)
 
* '''Partial cerebroside sulfate deficiency''':
 
* '''Pseudoarylsulfatase A deficiency''':
 
 
 
=== Cross-references ===
 
See also description of this disease in
 
* [http://en.wikipedia.org/wiki/Metachromatic_leukodystrophy Wikipedia article on MLD]
 
* [http://en.wikipedia.org/wiki/Arylsulfatase_A Wikipedia article on ARS A]
 
* [http://www.hgmd.cf.ac.uk/ac/gene.php?gene=ARSA HGMD entry of ARS A]
 
* [http://www.ncbi.nlm.nih.gov/omim/250100 OMIM entry for MLD]
 
* [http://www.ncbi.nlm.nih.gov/omim/607574 OMIM Entry for ARS A]
 
* [http://www.genome.jp/dbget-bin/www_bget?ds:H00127 KEGG disease entry for MLD]
 
 
 
== Biochemical disease mechanism ==
 
Arylsulfatase A is located in the Lysosome, where it is responsible for breaking up sulfated Glycosphingolipids (Sulfatides). As the sulfatides are not degraded, they build up and destroy the myelin sheath around the axons.
 
 
 
=== Cross-references ===
 
* [http://www.genome.jp/dbget-bin/www_bget?enzyme+3.1.6.8 KEGG entry of ARS A]
 
* [http://www.genome.jp/dbget-bin/www_bget?reaction+R04856+R06280 Reactions catalysed by ARS A]
 
* [MetaCyc reaction of ARS A]
 
 
== Mutations ==
 
[http://www.ncbi.nlm.nih.gov/omim/607574?report=Variants 47 known, disease causing allelic variants] are listed in the OMIM database.
 
 
Current knowledge about mutations associated with the disease. - Separate into disease causing and neutral mutations.
 
 
=== Reference sequence ===
 
 
Which sequence does not cause the disease and is most often found in the population.
 
* [[example_sequence|Create a page for the reference sequence.]] -- These sequence pages will be the starting point for collecting prediction results and result discussions.
 
 
=== Neutral mutations ===
 
* [[example_sequence|Create one page per mutated sequence]].
 
 
=== Disease causing mutations ===
 
* [[example_sequence|Create one page per mutated sequence]].
 
 
== References ==
 
<references />
 

Latest revision as of 23:02, 13 May 2011