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Ataxia due to vitamin E deficiency: A case report and updated review

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 b...

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Detalles Bibliográficos
Autores principales: Thapa, Sangharsha, Shah, Sangam, Chand, Swati, Sah, Sanjit Kumar, Gyawali, Pawan, Paudel, Sandip, Khanal, Pitambar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9448968/
https://www.ncbi.nlm.nih.gov/pubmed/36093469
http://dx.doi.org/10.1002/ccr3.6303
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author Thapa, Sangharsha
Shah, Sangam
Chand, Swati
Sah, Sanjit Kumar
Gyawali, Pawan
Paudel, Sandip
Khanal, Pitambar
author_facet Thapa, Sangharsha
Shah, Sangam
Chand, Swati
Sah, Sanjit Kumar
Gyawali, Pawan
Paudel, Sandip
Khanal, Pitambar
author_sort Thapa, Sangharsha
collection PubMed
description 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.
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spelling pubmed-94489682022-09-09 Ataxia due to vitamin E deficiency: A case report and updated review Thapa, Sangharsha Shah, Sangam Chand, Swati Sah, Sanjit Kumar Gyawali, Pawan Paudel, Sandip Khanal, Pitambar Clin Case Rep Case Report 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. John Wiley and Sons Inc. 2022-09-06 /pmc/articles/PMC9448968/ /pubmed/36093469 http://dx.doi.org/10.1002/ccr3.6303 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Thapa, Sangharsha
Shah, Sangam
Chand, Swati
Sah, Sanjit Kumar
Gyawali, Pawan
Paudel, Sandip
Khanal, Pitambar
Ataxia due to vitamin E deficiency: A case report and updated review
title Ataxia due to vitamin E deficiency: A case report and updated review
title_full Ataxia due to vitamin E deficiency: A case report and updated review
title_fullStr Ataxia due to vitamin E deficiency: A case report and updated review
title_full_unstemmed Ataxia due to vitamin E deficiency: A case report and updated review
title_short Ataxia due to vitamin E deficiency: A case report and updated review
title_sort ataxia due to vitamin e deficiency: a case report and updated review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9448968/
https://www.ncbi.nlm.nih.gov/pubmed/36093469
http://dx.doi.org/10.1002/ccr3.6303
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