Living donor liver transplantation for g
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Mureo Kasahara; Reiko Horikawa; Seisuke Sakamoto; Takanobu Shigeta; Hideaki Tana
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Article
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2009
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John Wiley and Sons
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English
โ 80 KB
Glycogen storage disease type 1b (GSD-1b) is due to an autosomal recessive inborn error of carbohydrate metabolism caused by defects in glucose-6-phosphatase translocase. Patients with GSD-1b have severe hypoglycemia with several clinical manifestations of hepatomegaly, obesity, a doll-like face, an