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
Successful Staged Kidney and Liver Transplantation for Glycogen Storage Disease Type Ib: A Case Report
โ Scribed by A.P. Martin; M. Bartels; S. Schreiber; P. Buehrdel; J. Hauss; J. Fangmann
- Book ID
- 116932974
- Publisher
- Elsevier Science
- Year
- 2006
- Tongue
- English
- Weight
- 560 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0041-1345
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Living donor liver transplantation for g
โ
Mureo Kasahara; Reiko Horikawa; Seisuke Sakamoto; Takanobu Shigeta; Hideaki Tana
๐
Article
๐
2009
๐
John Wiley and Sons
๐
English
โ 80 KB
Glycogen storage disease type I: indicat
โ
Labrune, Philippe
๐
Article
๐
2002
๐
Springer
๐
English
โ 310 KB
Glycogen storage disease type I: indicat
โ
Philippe Labrune
๐
Article
๐
2002
๐
Springer
๐
English
โ 61 KB
Hepatic adenomata in type Ia glycogen st
โ
C. Fontolliet; J.M. Matthieu; M. Gillet
๐
Article
๐
1998
๐
Elsevier Science
๐
English
โ 146 KB
Combined liver-kidney transplantation in
โ
Mirco Belingheri; Luciana Ghio; Ambra Sala; Francesca Menni; Laura Trespidi; Mar
๐
Article
๐
2007
๐
John Wiley and Sons
๐
English
โ 67 KB
Glycogen storage disease type Ia (GSD Ia) is a rare metabolic disorder due to hepatic glucose-6-phosphatase deficiency. Although great progress has been made in managing affected patients, severe hypoglycemia, lactic acidosis, hyperlipidemia, hepatic cytolysis, and impaired kidney function are frequ
Treatment with lenograstim (glycosylated
โ
A. Lachaux; O. Boillot; D. Stamm; I. Canterino; C. Dumontet; F. Regnier; D. Flor
๐
Article
๐
1993
๐
Elsevier Science
๐
English
โ 283 KB