Document Detail


Ornithine transcarbamoylase deficiency presenting with acute liver failure.
MedLine Citation:
PMID:  16802108     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Ornithine transcarbamoylase (OTC) deficiency is the most common hereditary urea cycle disorder. It is an X-linked recessive disorder that usually presents with encephalopathy and hyperammonaemia. We report a 14-month-old female carrier of OTC deficiency, who presented with a history of intermittent vomiting for 5 weeks and irritability and lethargy for 1 week. She was found to be in acute liver failure, with elevated transaminases, coagulopathy and a consistently low urea. Identifying an OTC mutation and ruling out other possible causes of acute hepatic failure confirmed the diagnosis. She was placed on low-protein diet supplemented with essential amino acids, and her liver enzymes, hyperammonaemia and coagulopathy corrected. Three other female patients have been reported with OTC deficiency presenting with severe cryptogenic hepatitis; our patient is unique in that the presentation of her disease was dominated by acute liver failure on a back ground of normal growth and development, no liver enlargement, and mild hyperammonaemia. OTC deficiency should be considered in the differential diagnosis of infants presenting with acute hepatocellular dysfunction, especially in females.
Authors:
Ahlam Mustafa; Joe T R Clarke
Related Documents :
24675018 - Alveolar capillary dysplasia with multiple congenital anomalies and bronchoscopic airwa...
8838298 - Ultrasound and cholangiography for the diagnosis of biliary complications after orthoto...
3513388 - Canine liver transplantation under nva2-cyclosporine versus cyclosporine.
3746598 - Infantile mammary duct ectasia: a cause of bloody nipple discharge.
10879648 - Pneumocystis carinii pneumonia in an immunocompetent infant with congenital cytomegalov...
18691938 - Neonatal circumcision in maryland: a comparison of hospital discharge and maternal post...
Publication Detail:
Type:  Case Reports; Journal Article     Date:  2006-06-26
Journal Detail:
Title:  Journal of inherited metabolic disease     Volume:  29     ISSN:  1573-2665     ISO Abbreviation:  J. Inherit. Metab. Dis.     Publication Date:  2006 Aug 
Date Detail:
Created Date:  2006-11-14     Completed Date:  2007-01-08     Revised Date:  2009-11-19    
Medline Journal Info:
Nlm Unique ID:  7910918     Medline TA:  J Inherit Metab Dis     Country:  Netherlands    
Other Details:
Languages:  eng     Pagination:  586     Citation Subset:  IM    
Affiliation:
Alberta Children's Hospital, University of Calgary, Calgary, Alberta, Canada, libra_dreams@yahoo.com.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Diet, Protein-Restricted
Female
Heterozygote
Humans
Hyperammonemia / etiology
Infant
Liver Failure, Acute / etiology*
Mutation
Ornithine Carbamoyltransferase / genetics
Ornithine Carbamoyltransferase Deficiency Disease* / diagnosis*,  diet therapy
Chemical
Reg. No./Substance:
EC 2.1.3.3/Ornithine Carbamoyltransferase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Subclinical course of adult visceral Niemann-Pick type C1 disease. A rare or underdiagnosed disorder...
Next Document:  Normal pregnancy outcome in L-2-hydroxyglutaric aciduria.