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Am J Med Genet A ; 185(3): 909-915, 2021 03.
Article in English | MEDLINE | ID: mdl-33369132

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.


Subject(s)
Alanine Transaminase/blood , Liver Diseases/etiology , Ornithine Carbamoyltransferase Deficiency Disease/complications , Age of Onset , Amino Acid Substitution , Aspartate Aminotransferases/blood , Biomarkers , Child, Preschool , Combined Modality Therapy , Developmental Disabilities/genetics , Disease Progression , Female , Hemorrhagic Disorders/etiology , Humans , Hyperammonemia/genetics , Infant , International Normalized Ratio , Liver Diseases/blood , Liver Diseases/surgery , Liver Transplantation , Mutation, Missense , Ornithine Carbamoyltransferase Deficiency Disease/blood , Ornithine Carbamoyltransferase Deficiency Disease/diet therapy , Ornithine Carbamoyltransferase Deficiency Disease/surgery , Vomiting/genetics
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