Glycogen storage disease with ventricular hypertrophy mimicking obstructive hypertrophic myocardiopathy
Glycogen storage disease type Ⅲ (GSD-Ⅲ) is an autosomal recessive inherited metabolic disorder caused by a deficiency in the glycogen debranching enzyme (amylo-l,6-glucosidase).1 The disease is characterized by hepatomegaly,fasting hypoglycemia,growth retardation,and progressive myopathy.1 It can also cause cardiomyopathy.1-5 We report a rare case of GSD-Ⅲ with metabolic cardiomyopathy mimicking obstructive hypertrophic cardiomyopathy, a sarcomere-protein gene disorder.
更多- 翻译满意度评价:
- 提交
- 浏览:105
- 被引:1
- 下载:4
相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文