| Literature DB >> 8535877 |
P Muiesan1, M Rela, P Kane, A Dawan, A Baker, C Ball, A P Mowat, R Williams, N D Heaton.
Abstract
Two cases of neonatal haemochromatosis, a rare and often fatal metabolic disorder, presenting with acute liver failure, are reported. Both presented in the first week of life with hypoglycaemia, jaundice, and coagulopathy, with rapid deterioration of liver function. Both received a transplantation using reduced liver grafts. One child was well 18 months later. Few survivors have been reported and despite the difficult perioperative management, liver transplantation is the best treatment for neonatal haemochromatosis.Entities:
Mesh:
Year: 1995 PMID: 8535877 PMCID: PMC2528468 DOI: 10.1136/fn.73.3.f178
Source DB: PubMed Journal: Arch Dis Child Fetal Neonatal Ed ISSN: 1359-2998 Impact factor: 5.747