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Ann Clin Neurophysiol > Volume 16(2); 2014 > Article
Ann Clin Neurophysiol. 2014; 16(2): 81-85.
Published online December 30, 2014.
doi: https://doi.org/10.14253/kjcn.2014.16.2.81
A Case of Adult Onset Glycogen Storage Myopathy
Jung Hwan Shin1, Dong Gun Kim1, Je Young Shin1, Sung Hye Park2, and Kwang Woo Lee1
1Departments of Neurology, Seoul National University College of Medicine, Seoul, Korea
2Departments of Pathology, Seoul National University College of Medicine, Seoul, Korea
Corresponding Author: Kwang Woo Lee ,Tel: +82-2-2072-3215 , Fax: +82-2-2072-7553, Email: kwoo@plaza.snu.ac.kr
Received April 7, 2014    Accepted December 5, 2014
Copyright © 2014 The Korean Society of Clinical Neurophysiology
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Primary metabolic myopathy as a type of congenital myopathies was first described by McArdle in 1951. Glycogen storage disease is a disease caused by genetic mutations involved in glycogen synthesis, glycogenolysis or glycolysis. Several types of glycogen storage disease are known to cause metabolic myopathies. We report a case of adult onset metabolic myopathy with glycogen storage.
Key words: Myopathy, Glycogen storage disease, Metabolic myopathy
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