| Literature DB >> 33369132 |
Kathryn Clarkston1,2, Joy Lee3,4, Sarah Donoghue4, Heidi Peters3,4, Hernan Eiroa5, Amit A Shah6,7, Kathleen Loomes6,7, Jessica Wen6,7, Mark Oliver3,8, Winita Hardikar3,8, Carlos E Prada1,9, Akihiro Asai1,2.
Abstract
We describe 10 females with ornithine transcarbamylase (OTC) deficiency and liver dysfunction, revealing a unique pattern of hepatocyte injury in which initial hyperammonemia and coagulopathy is followed by a delayed peak in aminotransferase levels. None of the patients required urgent liver transplantation, though five eventually underwent transplant for recurrent metabolic crises. We intend that this novel observation will initiate further investigations into the pathophysiology of liver dysfunction in OTC-deficient patients, and ultimately lead to the development of therapies and prevent the need for liver transplant.Entities:
Keywords: acute liver dysfunction; female manifestation of OTC deficiency; hepatic lyonization; hyperammonemia; ornithine transcarbamylase
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Year: 2020 PMID: 33369132 PMCID: PMC7974766 DOI: 10.1002/ajmg.a.62031
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802