Familial isolated vitamin E deficiency
| Familial isolated vitamin e deficiency | |
|---|---|
| Other names | Ataxia With Vitamin E Deficiency |
 | |
| Familial isolated vitamin e deficiency has an autosomal recessive pattern of inheritance. | |
| Specialty | Neurology  |
Familial Isolated Vitamin E Deficiency is a rare autosomal recessive neurodegenerative disease.[1][2][3][4] 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.[5]
Diagnosis
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Treatment
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See also
References
- ^ "Ataxia with vitamin E deficiency". www.orpha.net. Retrieved 2017-01-19.
- ^ Doerflinger N, Linder C, Ouahchi K, Gyapay G, Weissenbach J, Le Paslier D, Rigault P, Belal S, Ben Hamida C, Hentati F (May 1995). "Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families" (Free full text). American Journal of Human Genetics. 56 (5): 1116–24. ISSN 0002-9297. PMC 1801469. PMID 7726167.
- ^ Reference, Genetics Home. "ataxia with vitamin E deficiency". Genetics Home Reference. Retrieved 2017-01-19.
- ^ Schuelke, Markus (1993-01-01). "Ataxia with Vitamin e Deficiency". In Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora JH; Bird, Thomas D.; Ledbetter, Nikki; Mefford, Heather C. (eds.). GeneReviews. Seattle (WA): University of Washington, Seattle. PMID 20301419.
- ^ Template:Fitness Hacker[permanent dead link]
External links
- Ataxia with vitamin E deficiency at NIH's Office of Rare Diseases
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