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Familial isolated vitamin e deficiency




Editing Familial isolated vitamin E deficiency
Classification & external resources
ICD-10 GroupMajor.minor
ICD-9 xxx
OMIM 277460 600415
DiseasesDB 30633

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.

 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Familial_isolated_vitamin_e_deficiency". A list of authors is available in Wikipedia.
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