Difference between revisions of "Metachromatic leukodystrophy"

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m (Created page with "== Summary == The example disease causes the example syndrome. Metachromatic leukodystrophy (MLD) is a genetic disorder that affects nerves, muscles, other organs, and behavior.…")
 
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== Phenotype ==
 
== Phenotype ==
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The disease leads to a toxic buildup of lipids in cells in the nervous system, liver, and kidneys (see below for mechanism). The disease affects the muscle tone, leading to abnormally high muscle tone as well as decreased muscle tone. This in turn leads to walking and feeding difficulties, frequent falls, incontinence, speech difficulties with slurring, etc. It can also effect nerve function and lead to decreased mental function, personality changes, etc. (see [http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0002185/ PubMed Health]).
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There are three forms of MLD: late infantile, juvenile, and adult (see [National Institute of Neurological Disorders and Stroke http://www.ninds.nih.gov/disorders/metachromatic_leukodystrophy/metachromatic_leukodystrophy.htm]).
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* The ''late infantile form'' is most common ([http://ghr.nlm.nih.gov/condition/metachromatic-leukodystrophy 50 to 60 per cent of patients]). It sets in between 12 and 20 months following birth. Affected children have difficulty walking after the first year of life and subsequently show muscle wasting leading to paralysis, loss of vision leading to blindness, and dementia. Most children with this form of MLD die by age 5.
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* The ''juvenile form'' sets in between 3-10 years of age. It usually begins with impaired school performance. Subsequently symptoms similar to the late infantile form occur, but with slower progression. Death occurs 10 to 20 years following the onset of the disease.
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* The ''adult form'' commonly begins after age 16. It is first seen as a psychiatric disorder or progressive dementia. Symptoms include impaired concentration, ataxia, seizures, dementia, and tremor. Death occurs 6 to 14 years following the onset of the disease.
   
The disease affects the muscle tone, leading to abnormally high muscle tone as well as decreased muscle tone. This in turn leads to walking and feeding difficulties, frequent falls, incontinence, speech difficulties with slurring, etc. It can also effect nerve function and lead to decreased mental function, personality changes, etc. (see [http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0002185/ PubMed Health].
 
   
   

Revision as of 14:29, 29 March 2012

Summary

The example disease causes the example syndrome.

Metachromatic leukodystrophy (MLD) is a genetic disorder that affects nerves, muscles, other organs, and behavior. It slowly gets worse over time.

Phenotype

The disease leads to a toxic buildup of lipids in cells in the nervous system, liver, and kidneys (see below for mechanism). The disease affects the muscle tone, leading to abnormally high muscle tone as well as decreased muscle tone. This in turn leads to walking and feeding difficulties, frequent falls, incontinence, speech difficulties with slurring, etc. It can also effect nerve function and lead to decreased mental function, personality changes, etc. (see PubMed Health).

There are three forms of MLD: late infantile, juvenile, and adult (see [National Institute of Neurological Disorders and Stroke http://www.ninds.nih.gov/disorders/metachromatic_leukodystrophy/metachromatic_leukodystrophy.htm]).

  • The late infantile form is most common (50 to 60 per cent of patients). It sets in between 12 and 20 months following birth. Affected children have difficulty walking after the first year of life and subsequently show muscle wasting leading to paralysis, loss of vision leading to blindness, and dementia. Most children with this form of MLD die by age 5.
  • The juvenile form sets in between 3-10 years of age. It usually begins with impaired school performance. Subsequently symptoms similar to the late infantile form occur, but with slower progression. Death occurs 10 to 20 years following the onset of the disease.
  • The adult form commonly begins after age 16. It is first seen as a psychiatric disorder or progressive dementia. Symptoms include impaired concentration, ataxia, seizures, dementia, and tremor. Death occurs 6 to 14 years following the onset of the disease.


Cross-references

See also description of this disease in

  • specific link to Wikipedia
  • specific link to HGMD
  • specific link to OMIM

... (see databases in "resources")

Biochemical disease mechanism

The example protein is involved in the example pathway...

Ideally, include a graphical pathway representation like this one:

Sphingolipid Metabolism (source: KEGG) highlighting disease associated enzymes

(see above: own words, no plagiarism)


Cross-references

  • link to KEGG
  • link to MetaCyc

... see databases in "resources"