Complete Information on Andersen Tawil syndrome with Treatment and Prevention
Andersen tawil syndrome is a rare genetic disorder, its occurrence is unknown. Anderson the tawil synthesis symptom is causes the periodic paralysis plot the confusion, change in heart rhythm, with development abnormality.
This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. In some cases, a person with Andersen tawil syndrome inherits the mutation from one affected parent. These cases occur in people with no history of the disorder in their family. There may be several variant mutations, producing similar but slightly different forms of the disorder, as occurs in the other forms of periodic paralysis, where several variants of each type have been identified.
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