Pathological characteristics of glycogen storage disease III in skeletal muscle
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- 作者：Leah D. Gershenb ; Brigid E. Praysonc ; Richard A. Praysona ; praysor@ccf.org" class="auth_mail" title="E-mail the corresponding author
- 关键词：Cori disease ; Debrancher enzyme deficiency ; Glycogenosis III ; Skeletal muscle biopsy
- 刊名：Journal of Clinical Neuroscience
- 出版年：2015
- 出版时间：October 2015
- 年：2015
- 卷：22
- 期：10
- 页码：1674-1675
- 全文大小：942 K
文摘
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Certain glycogenoses, including Type III, result in vacuolar myopathic changes.
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Glycogen storage disease III is an autosomal recessive condition.
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Glycogen storage disease III typically involves both skeletal muscle and liver.