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Glycogen-Storage Disease Type I - In 1929, von Gierke provided the initial description of glycogen-storage disease type I (GSD I) from autopsy reports of 2 children whose very large livers contained excessive glycogen. (He also reported similar findings in the kidneys.) Both children had frequent nosebleeds prior to death, consistent with histories documented in today's patients.In 1952, Cori and Cori reported a series of 6 similar patients. Two had almost total deficiency of hepatic glucose-6-phosphatase, while the remaining 4 had ...

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Glycogen Storage Disease Type I

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Glycogen

not-for-profit foundation committed to funding research so that children born with GSD1 will benefit from early detection, treatment, and an eventual cure

Health care centre, teaching and research hospital - Vancouver Hospital and Health Sciences Centre in British Columbia Canada.

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