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Familial Isolated Vitamin E Deficiency is a rare, autosomal recessive neurodegenerative disease. Symptoms are similar to those of Friedreich ataxia.

Cause

Familial Isolated Vitamin E Deficiency is caused by mutations in the gene for a-tocopherol transfer protein.

Familial isolated vitamin e deficiency has an autosomal recessive pattern of inheritance.

External Links

• Ataxia with vitamin E deficiency at NIH's Office of Rare Diseases
• aved at NIH/UW GeneTests

This genetic disorder article is a stub. You can help Wikipedia by expanding it.

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