Living donor liver transplantation for Wilson’s disease from a compound heterozygote donor with a low ceruloplasmin level: a case report

Wilson’s disease (WD) is an autosomal recessive disorder resulting from mutations in the ATP7B gene. When chelation therapy proves ineffective, liver transplantation serves as the definitive treatment option. However, owing to the scarcity of cadaveric donor organs, living donor liver transplantatio...

Deskribapen osoa

Xehetasun bibliografikoak

Egile Nagusiak:	Hsin-Yen Chou, Chia-Feng Yang, Cheng-Yen Chen, Hsin-Lin Tsai, Hao-Jan Lei, Yi-Fan Tsou, Fang-Cheng Kuo, Meng-Hsuan Chung, Cheng-Yuan Hsia, Shu-Cheng Chou, Shen-Chih Wang, Chin-Su Liu, Niang-Cheng Lin
Formatua:	Artigo
Hizkuntza:	Inglês
Argitaratua:	Elsevier 2026-02-01
Saila:	Transplantation Reports
Gaiak:	Liver transplantation Living donor liver transplantation Wilson’s disease
Sarrera elektronikoa:	http://www.sciencedirect.com/science/article/pii/S2451959625000204
Etiketak:	Etiketa erantsi Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!