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Turk J Pediatr ; 50(5): 471-5, 2008.
Article in English | MEDLINE | ID: mdl-19102053

ABSTRACT

Ataxia with vitamin E deficiency (AVED) is a rare autosomal recessive disorder, usually with a phenotype resembling Friedreich ataxia, caused by selective impairment of gastrointestinal vitamin E absorption. Vitamin E supplementation improves symptoms and prevents disease progress. In North Africa and Southern Europe, AVED is as common as Friedreich ataxia. There are no reported cases from Turkey. We herein report a 16-year-old Turkish girl with AVED, who was found to have total deletion of the TTPA gene as well as sensorineural deafness, and we present her follow-up data after vitamin E therapy.


Subject(s)
Ataxia/complications , Deafness/complications , Vitamin E Deficiency/complications , Adolescent , Amino Acid Sequence , Ataxia/blood , Ataxia/genetics , Carrier Proteins/genetics , Deafness/blood , Deafness/genetics , Female , Humans , Phenotype , Polymerase Chain Reaction , RNA, Messenger/genetics , Sequence Deletion , Vitamin E/blood , Vitamin E Deficiency/blood , Vitamin E Deficiency/genetics
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