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Muscle Biopsy: A Boon for Diagnosis of Mitochondrial Parkinsonism in Developing Countries
Mitochondrial dysfunction plays an important role in the pathogenesis of Parkinson's disease. Primary genetic abnormalities in the mitochondrial DNA or nuclear DNA can cause parkinsonism. Mitochondrial parkinsonism presents with classical features of parkinsonism along with multisystem involvem...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6472221/ https://www.ncbi.nlm.nih.gov/pubmed/31007443 http://dx.doi.org/10.4103/aian.AIAN_436_17 |
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author | Shree, Ritu Mehta, Sahil Goyal, Manoj K Gaspar, Balan L Lal, Vivek |
author_facet | Shree, Ritu Mehta, Sahil Goyal, Manoj K Gaspar, Balan L Lal, Vivek |
author_sort | Shree, Ritu |
collection | PubMed |
description | Mitochondrial dysfunction plays an important role in the pathogenesis of Parkinson's disease. Primary genetic abnormalities in the mitochondrial DNA or nuclear DNA can cause parkinsonism. Mitochondrial parkinsonism presents with classical features of parkinsonism along with multisystem involvement. Genetic analysis is essential in reaching the diagnosis which is not always possible, especially in developing countries. Muscle biopsy can be a boon in this setting as exemplified in our report of two siblings where a diagnosis of mitochondrial parkinsonism was made on the basis of muscle biopsy. |
format | Online Article Text |
id | pubmed-6472221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-64722212019-04-19 Muscle Biopsy: A Boon for Diagnosis of Mitochondrial Parkinsonism in Developing Countries Shree, Ritu Mehta, Sahil Goyal, Manoj K Gaspar, Balan L Lal, Vivek Ann Indian Acad Neurol Case Reports Mitochondrial dysfunction plays an important role in the pathogenesis of Parkinson's disease. Primary genetic abnormalities in the mitochondrial DNA or nuclear DNA can cause parkinsonism. Mitochondrial parkinsonism presents with classical features of parkinsonism along with multisystem involvement. Genetic analysis is essential in reaching the diagnosis which is not always possible, especially in developing countries. Muscle biopsy can be a boon in this setting as exemplified in our report of two siblings where a diagnosis of mitochondrial parkinsonism was made on the basis of muscle biopsy. Wolters Kluwer - Medknow 2019 /pmc/articles/PMC6472221/ /pubmed/31007443 http://dx.doi.org/10.4103/aian.AIAN_436_17 Text en Copyright: © 2006 - 2019 Annals of Indian Academy of Neurology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Reports Shree, Ritu Mehta, Sahil Goyal, Manoj K Gaspar, Balan L Lal, Vivek Muscle Biopsy: A Boon for Diagnosis of Mitochondrial Parkinsonism in Developing Countries |
title | Muscle Biopsy: A Boon for Diagnosis of Mitochondrial Parkinsonism in Developing Countries |
title_full | Muscle Biopsy: A Boon for Diagnosis of Mitochondrial Parkinsonism in Developing Countries |
title_fullStr | Muscle Biopsy: A Boon for Diagnosis of Mitochondrial Parkinsonism in Developing Countries |
title_full_unstemmed | Muscle Biopsy: A Boon for Diagnosis of Mitochondrial Parkinsonism in Developing Countries |
title_short | Muscle Biopsy: A Boon for Diagnosis of Mitochondrial Parkinsonism in Developing Countries |
title_sort | muscle biopsy: a boon for diagnosis of mitochondrial parkinsonism in developing countries |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6472221/ https://www.ncbi.nlm.nih.gov/pubmed/31007443 http://dx.doi.org/10.4103/aian.AIAN_436_17 |
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