A retrospective longitudinal study and comprehensive review of adult patients with glycogen storage disease type III

Introduction: A deficiency of glycogen debrancher enzyme in patients with glycogen storage disease type III (GSD III) manifests with hepatic, cardiac, and muscle involvement in the most common subtype (type a), or with only hepatic involvement in patients with GSD IIIb. Objective and methods: To des...

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Autores principales:	Ghada Hijazi, Anna Paschall, Sarah P. Young, Brian Smith, Laura E. Case, Tracy Boggs, Sathya Amarasekara, Stephanie L. Austin, Surekha Pendyal, Areeg El-Gharbawy, Kristen L. Deak, Andrew J. Muir, Priya S. Kishnani
Formato:	article
Lenguaje:	EN
Publicado:	Elsevier 2021
Materias:	Glycogen storage disease type III (GSD III) Hypoglycemia Cirrhosis Left ventricular hypertrophy (LVH) Cardiomyopathy and myopathy Medicine (General) R5-920 Biology (General) QH301-705.5
Acceso en línea:	https://doaj.org/article/4e0ccde04a5d4a4db4785200b06ae36a
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A retrospective longitudinal study and comprehensive review of adult patients with glycogen storage disease type III

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