ICD-9 / Health Information

Familial isolated vitamin e deficiency

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From Wikipedia, the free encyclopedia

| ICD9 = | ICDO = | OMIM = 277460 | OMIM_mult = | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = Familial Isolated Vitamin E Deficiency is a rare autosomal recessive neurodegenerative disease. Symptoms are much like those of Friedreich ataxia and is caused by mutations in the gene for a-tocopherol transfer protein. ''' Ataxia is due to vitamin deficiency, If you suffer from any kind of ataxia, i suggest you try takin vitamin e capsules.

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