Baussan C, Moatti N, Lemonnier A
Laboratoire central de Biochimie, Hôpital Bicêtre, Le Kremlin-Bicêtre.
Ann Gastroenterol Hepatol (Paris). 1988 Mar-Apr;24(2):63-7.
Liver glycogenosis (GSD) are hereditary diseases caused by deficiencies of the three major enzymatic systems involved in glycogenolysis: glucose-6-phosphatase (GSD I), debranching enzyme (GSD III) and phosphorylase system (GSD VI). Biological and physiopathological aspects of these disorders are described. An up to date diagnostic process which includes measurement of glycogen and enzymatic activities, in the most appropriate tissue material, is proposed.
肝糖原贮积症(GSD)是由糖原分解所涉及的三大酶系统缺乏引起的遗传性疾病:葡萄糖-6-磷酸酶(GSD I型)、脱支酶(GSD III型)和磷酸化酶系统(GSD VI型)。描述了这些疾病的生物学和病理生理学方面。提出了一种最新的诊断方法,包括在最合适的组织材料中测量糖原和酶活性。