
Ataxia due to vitamin E deficiency: A case report and updated review
Author(s) -
Thapa Sangharsha,
Shah Sangam,
Chand Swati,
Sah Sanjit Kumar,
Gyawali Pawan,
Paudel Sandip,
Khanal Pitambar
Publication year - 2022
Publication title -
clinical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 9
ISSN - 2050-0904
DOI - 10.1002/ccr3.6303
Subject(s) - ataxia , medicine , pediatrics , disease , audiology , pathology , psychiatry
Ataxia with vitamin E deficiency (AVED) is a rare cause of hereditary ataxia in developing countries with unknown prevalence. AVED is an autosomal‐recessive disorder, which is characterized by ataxia, areflexia, and proprioceptive and vibratory sensory loss. The disease is characterized clinically by symptoms with often resembling to those of Friedreich ataxia (FRDA). Vitamin E supplementation improves symptoms and prevents the progression of the disease. In this case report, we reviewed the recently updated findings in AVED in regard to the management and present a case of AVED in a 16‐year‐old boy, who was initially misdiagnosed as FRDA, prior to the genetic test.