Year: 1999
Type: article
Study design: Case Report
Abstract: #### Background
Haemochromatosis is a common genetic disease leading to iron overload. Although the gene had been identified ( HFE ),1 the pathogenesis had not been fully elucidated.2 The inadvertent transplant of a C282Y homozygous liver and intestine provided a unique opportunity to study this problem.
##### Methods
A 19 year old man underwent orthotopic liver and intestinal transplantation in January 1997 for the treatment of short bowel syndrome secondary to a mid gut volvulus with resection and cholestatic liver disease resulting from total parenteral nutrition. The organ donor was an 18 year old woman posthumously discovered to be a C282Y homozygote for haemochromatosis.
##### Results
Preoperative recipient …
Source: Gut
DOI: 10.1136/gut.45.5.783
Authors: P C ADAMS, G JEFFREY, K ALANEN, S CHAKRABARTI, R PRESHAW, W HOWSON, D GRANT
Institutions: Western University, University of Calgary
Language: English
Subfield: Hematology
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
OpenAlex ID: W2120753299
