Difference between revisions of "Fabry Disease 2011"
From Bioinformatikpedia
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== Biochemical disease mechanism == |
== Biochemical disease mechanism == |
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| + | [[Image:Fabry_disease_glycosphingolipid_pathway.png|thumb|right|Glycosphingolipid biosynthesis of Homo sapiens. The disease associated enzyme is highlighted in red.]] |
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=== Cross-references === |
=== Cross-references === |
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* [http://www.genome.jp/dbget-bin/www_bget?ds:H00125 KEGG: Fabry Disease] |
* [http://www.genome.jp/dbget-bin/www_bget?ds:H00125 KEGG: Fabry Disease] |
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Revision as of 00:02, 15 May 2011
Contents
Summary
Phenotype
Symptoms
As the effects caused by the enzymatic disfunction summarize over time, the symptoms evolve progressive.
Childhood
- Pain and burning in the hands and feet
- Impaired sweating
- Psychological and social issues
- Low tolerance for exercise
- Eye abnormalities
Adolescence
- Dark red skin rashes (angiokeratomas[1])
- Fatigue
- Gastrointestinal problems
Adulthood
- Heart problems
- Kidney problems
- Nervous system problems
- Hearing problems
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
Cross-references
Mutations
Current knowledge about mutations associated with the disease. - Separate into disease causing and neutral mutations. -- These sequence pages will be the starting point for collecting prediction results and result discussions.
Note: Currently (13.5.) you only need to care about the reference sequence pages. -- At a later stage we will assign mutations we expect you to work on. Then, it will make sense to create on page per mutation that is assigned to you.
Reference sequence
Which sequence does not cause the disease and is most often found in the population.
