Tay-Sachs Disease 2011
The Tay-Sachs disease (TSD) is a rare autosomal, recessive genetic disorder which is caused by accumulation of lipids in the brain. This leads to the cell death of those neurons. There exist three different variations of the TSD. The most common one is the Infantile Tay-Sachs disease which affects death of the children under the age of 5. The two other variants are the Juvenile and Adult/Late Onset TSD, which are less aggressive. The disease causes a deterioration of mental and physical abilities. Sadly, there currently exists no treatment.
The most common and aggressive form of TSD is the infantile TSD, which has a lot of different symptoms and leads to the early death of the affected children. The most common symptoms are: - normal development in the first six month after birth - "cherry-red" macula - paralysis - dementia - blindness - deafness - muscle atrophy - startle response to sound stimuli - inability to coordinate muscle movement (child can't roll over and sit) - death in the second or third year
Juvenile and Adult TSD: This forms of the Tay-Sachs disease occur later in lifetime. These two forms were not always recogniced as variants of the TSD. The symptomes of these forms are less aggressive. Often the patients become wheelchair users and have some psychiatric and physical limitation, which could be handled with drugs.
See also description of this disease in     
Biochemical disease mechanism
The example protein is involved in the example pathway...
Ideally, include a graphical pathway representation like this one:
(see above: own words, no plagiarism)
- link to KEGG
- link to MetaCyc
... see databases in "resources"
Current knowledge about mutations associated with the disease. - Separate into disease causing and neutral mutations.
Which sequence does not cause the disease and is most often found in the population.
- Create a page for the reference sequence. -- These sequence pages will be the starting point for collecting prediction results and result discussions.