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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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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. |
format | Online Article Text |
id | pubmed-9448968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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