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
โฆ LIBER โฆ
Outcome of living donor liver transplantation for glycogen storage disease
โ Scribed by P.-P Liu; V.H de Villa; Y.-S Chen; C.-C Wang; S.-H Wang; Y.-C Chiang; B Jawan; H.-K Cheung; Y.-F Cheng; T.-L Huang; H.-L Eng; F.-R Chuang; C.-L Chen
- Book ID
- 117233049
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- English
- Weight
- 56 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0041-1345
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