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
Glycogen storage disease type I: indications for liver and/or kidney transplantation
โ Scribed by Philippe Labrune
- Publisher
- Springer
- Year
- 2002
- Tongue
- English
- Weight
- 61 KB
- Volume
- 161
- Category
- Article
- ISSN
- 0340-6997
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