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Calf heads on a trophy sign: Miyoshi myopathy

Miyoshi myopathy is an autosomal recessive distal myopathy with predominant involvement of the posterior calf muscles attributed to mutations in the dysferlin gene. We report a 26-year-old male, born of nonconsanginous parentage. He noticed weakness and atrophy of leg muscles with inability to walk...

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Autores principales: Shyma, M. Mundayadan, Roopchand, P. Sreedharan, Ram, K. Mohan, Shaji, C. Velayudhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481807/
https://www.ncbi.nlm.nih.gov/pubmed/26167036
http://dx.doi.org/10.4103/0976-3147.158798
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author Shyma, M. Mundayadan
Roopchand, P. Sreedharan
Ram, K. Mohan
Shaji, C. Velayudhan
author_facet Shyma, M. Mundayadan
Roopchand, P. Sreedharan
Ram, K. Mohan
Shaji, C. Velayudhan
author_sort Shyma, M. Mundayadan
collection PubMed
description Miyoshi myopathy is an autosomal recessive distal myopathy with predominant involvement of the posterior calf muscles attributed to mutations in the dysferlin gene. We report a 26-year-old male, born of nonconsanginous parentage. He noticed weakness and atrophy of leg muscles with inability to walk on his heels. The creatine kinase concentration was high. The electromyography showed myopathic pattern and the muscle biopsy disclosed dystrophic changes with absence of dysferlin. Miyoshi myopathy may be distinct among the hereditary distal myopathies. There are only few reported cases of Miyoshi myopathy in the world literature. In India only 12 cases were reported who had classical features of Miyoshi myopathy. Our's is a typical case of Miyoshi myopathy, with an affected twin sister as well. He also had “calf heads on a trophy sign” on physical examination, which is considered to be pathognomonic of this disease.
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spelling pubmed-44818072015-07-12 Calf heads on a trophy sign: Miyoshi myopathy Shyma, M. Mundayadan Roopchand, P. Sreedharan Ram, K. Mohan Shaji, C. Velayudhan J Neurosci Rural Pract Case Report Miyoshi myopathy is an autosomal recessive distal myopathy with predominant involvement of the posterior calf muscles attributed to mutations in the dysferlin gene. We report a 26-year-old male, born of nonconsanginous parentage. He noticed weakness and atrophy of leg muscles with inability to walk on his heels. The creatine kinase concentration was high. The electromyography showed myopathic pattern and the muscle biopsy disclosed dystrophic changes with absence of dysferlin. Miyoshi myopathy may be distinct among the hereditary distal myopathies. There are only few reported cases of Miyoshi myopathy in the world literature. In India only 12 cases were reported who had classical features of Miyoshi myopathy. Our's is a typical case of Miyoshi myopathy, with an affected twin sister as well. He also had “calf heads on a trophy sign” on physical examination, which is considered to be pathognomonic of this disease. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4481807/ /pubmed/26167036 http://dx.doi.org/10.4103/0976-3147.158798 Text en Copyright: © Journal of Neurosciences in Rural Practice http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Shyma, M. Mundayadan
Roopchand, P. Sreedharan
Ram, K. Mohan
Shaji, C. Velayudhan
Calf heads on a trophy sign: Miyoshi myopathy
title Calf heads on a trophy sign: Miyoshi myopathy
title_full Calf heads on a trophy sign: Miyoshi myopathy
title_fullStr Calf heads on a trophy sign: Miyoshi myopathy
title_full_unstemmed Calf heads on a trophy sign: Miyoshi myopathy
title_short Calf heads on a trophy sign: Miyoshi myopathy
title_sort calf heads on a trophy sign: miyoshi myopathy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481807/
https://www.ncbi.nlm.nih.gov/pubmed/26167036
http://dx.doi.org/10.4103/0976-3147.158798
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