A Case of Glycogen Storage Disease IV with Rare Homozygous Mutations in the Glycogen Branching Enzyme Gene

  • Choi, So Yoon
  • Kang, Ben
  • Choe, Jae Young
  • Lee, Yoon
  • Jang, Hyo Jeong
  • 외 3명
Citations

WEB OF SCIENCE

5
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SCOPUS

8

초록

Glycogen storage disease (GSD) IV is a rare autosomal recessive inherited disorder caused by mutations in the gene coding for glycogen branching enzyme leading to progressive liver disease. GSD IV is associated with mutations in GBE1, which encodes the glycogen branching enzyme. We report a case of GSD IV with rare homozygous mutations in the GBE1 gene (c.791G>A (p.Gly264Glu), which was successfully treated by liver transplantation.

키워드

Andersen diseaseGlycogen branching enzymeLiver transplantationLIVER-TRANSPLANTATION
제목
A Case of Glycogen Storage Disease IV with Rare Homozygous Mutations in the Glycogen Branching Enzyme Gene
저자
Choi, So YoonKang, BenChoe, Jae YoungLee, YoonJang, Hyo JeongPark, Hyung-DooLee, Suk-KooChoe, Yon Ho
DOI
10.5223/pghn.2018.21.4.365
발행일
2018-10
유형
Article
저널명
Pediatric Gastroenterology, Hepatology & Nutrition
21
4
페이지
365 ~ 368