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Myopathies of endocrine disorders: A prospective clinical and biochemical study

INTRODUCTION: Major categories of endocrine myopathy include those associated with: Adrenal dysfunction (as in Cushing's disease or steroid myopathy); thyroid dysfunction (as in myxedema coma or thyrotoxic myopathy); vitamin D deficiency; parathyroid dysfunction; and pituitary dysfunction. Ster...

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Autores principales: Sharma, Vikas, Borah, Papori, Basumatary, Lakshya J., Das, Marami, Goswami, Munindra, Kayal, Ashok K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162016/
https://www.ncbi.nlm.nih.gov/pubmed/25221399
http://dx.doi.org/10.4103/0972-2327.138505
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author Sharma, Vikas
Borah, Papori
Basumatary, Lakshya J.
Das, Marami
Goswami, Munindra
Kayal, Ashok K.
author_facet Sharma, Vikas
Borah, Papori
Basumatary, Lakshya J.
Das, Marami
Goswami, Munindra
Kayal, Ashok K.
author_sort Sharma, Vikas
collection PubMed
description INTRODUCTION: Major categories of endocrine myopathy include those associated with: Adrenal dysfunction (as in Cushing's disease or steroid myopathy); thyroid dysfunction (as in myxedema coma or thyrotoxic myopathy); vitamin D deficiency; parathyroid dysfunction; and pituitary dysfunction. Steroid myopathy is the most common endocrine myopathy. OBJECTIVE: To study the etiology, varied presentations, and outcome after therapy of patients with endocrine myopathies. MATERIALS AND METHODS: Myopathy was evaluated by the standard clinical procedures: Detailed clinical history, manual muscle strength testing, and creatine phosphokinase (CPK). Endocrine disorders were diagnosed as per clinical features and biochemical parameters. The treatment was given to patients as per underlying endocrine disease. Myopathy was assessed before and after treatment. RESULTS: Out of the 37 patients who were diagnosed with endocrine myopathies, thyroid dysfunction was the most common cause (17 cases), followed by vitamin D deficiency in nine, adrenal dysfunction in six, parathyroid dysfunction in three, and pituitary dysfunction in two. Some patients had atypical presentation (repeated falls in one, tongue fasciculations in one, neck weakness in five, one with ptosis and facial weakness, asymmetrical onset in one, and calf hypertrophy in one. The serum creatine kinase (CK) concentration did not correlate with muscle weakness. Following the treatment regimen which was specific for a given myopathy, 26 patients recovered fully. CONCLUSION: We found varied clinical presentations of endocrine myopathies. All the patients with neuromuscular complaints should be investigated for endocrine causes because significant number of them recovers fully with specific treatment.
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spelling pubmed-41620162014-09-14 Myopathies of endocrine disorders: A prospective clinical and biochemical study Sharma, Vikas Borah, Papori Basumatary, Lakshya J. Das, Marami Goswami, Munindra Kayal, Ashok K. Ann Indian Acad Neurol Original Article INTRODUCTION: Major categories of endocrine myopathy include those associated with: Adrenal dysfunction (as in Cushing's disease or steroid myopathy); thyroid dysfunction (as in myxedema coma or thyrotoxic myopathy); vitamin D deficiency; parathyroid dysfunction; and pituitary dysfunction. Steroid myopathy is the most common endocrine myopathy. OBJECTIVE: To study the etiology, varied presentations, and outcome after therapy of patients with endocrine myopathies. MATERIALS AND METHODS: Myopathy was evaluated by the standard clinical procedures: Detailed clinical history, manual muscle strength testing, and creatine phosphokinase (CPK). Endocrine disorders were diagnosed as per clinical features and biochemical parameters. The treatment was given to patients as per underlying endocrine disease. Myopathy was assessed before and after treatment. RESULTS: Out of the 37 patients who were diagnosed with endocrine myopathies, thyroid dysfunction was the most common cause (17 cases), followed by vitamin D deficiency in nine, adrenal dysfunction in six, parathyroid dysfunction in three, and pituitary dysfunction in two. Some patients had atypical presentation (repeated falls in one, tongue fasciculations in one, neck weakness in five, one with ptosis and facial weakness, asymmetrical onset in one, and calf hypertrophy in one. The serum creatine kinase (CK) concentration did not correlate with muscle weakness. Following the treatment regimen which was specific for a given myopathy, 26 patients recovered fully. CONCLUSION: We found varied clinical presentations of endocrine myopathies. All the patients with neuromuscular complaints should be investigated for endocrine causes because significant number of them recovers fully with specific treatment. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4162016/ /pubmed/25221399 http://dx.doi.org/10.4103/0972-2327.138505 Text en Copyright: © Annals of Indian Academy of Neurology 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 Original Article
Sharma, Vikas
Borah, Papori
Basumatary, Lakshya J.
Das, Marami
Goswami, Munindra
Kayal, Ashok K.
Myopathies of endocrine disorders: A prospective clinical and biochemical study
title Myopathies of endocrine disorders: A prospective clinical and biochemical study
title_full Myopathies of endocrine disorders: A prospective clinical and biochemical study
title_fullStr Myopathies of endocrine disorders: A prospective clinical and biochemical study
title_full_unstemmed Myopathies of endocrine disorders: A prospective clinical and biochemical study
title_short Myopathies of endocrine disorders: A prospective clinical and biochemical study
title_sort myopathies of endocrine disorders: a prospective clinical and biochemical study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162016/
https://www.ncbi.nlm.nih.gov/pubmed/25221399
http://dx.doi.org/10.4103/0972-2327.138505
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