ataxia with vitamin E deficiency(English)

• a rare autosomal recessive condition that is caused by a mutation in the alpha tocopherol transfer protein gene, and characterized by progressive cerebellar ataxia, dorsal column signs, and pyramidal deficits on examination
• ARCA, ARSACS, SACS, SCAR, SYNE
• Ataxia, Hormone, Neuropathy, Congenital disorders, Spine (or spinal cord), Vitamin
• https://doi.org…55/2016/8342653