Successful combined liver/kidney transplantation from a donor with Pompe disease.

Abstract:

:Pompe disease results from inherited deficiency of the enzyme acid alpha-glucosidase resulting in lysosomal accumulation of glycogen primarily in skeletal muscle. Reported is the first case in which a donor with late onset Pompe disease (LOPD) was successfully used for deceased donor liver and kidney transplantation. This case demonstrates co-operative transplant surgery and genetic medicine evaluation and risk estimation for donors with inherited metabolic disorders some of which may be suitable for donation of selected organs for transplantation.

journal_name

Mol Genet Metab

authors

Halldorson J,Kazi Z,Mekeel K,Kuo A,Hassanein T,Loomba R,Austin S,Valasek MA,Kishnani P,Hemming AW

doi

10.1016/j.ymgme.2015.05.007

subject

Has Abstract

pub_date

2015-08-01 00:00:00

pages

141-4

issue

4

eissn

1096-7192

issn

1096-7206

pii

S1096-7192(15)30014-7

journal_volume

115

pub_type

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