Article info
PDFNeurological rarities
Urea cycle disorders: a life-threatening yet treatable cause of metabolic encephalopathy in adults
- Correspondence to Dr Michel C Tchan, Department of Genetic Medicine, Westmead Hospital, Hawkesbury Road, Westmead NSW 2145, Australia; michel.tchan{at}health.nsw.gov.au
Citation
Urea cycle disorders: a life-threatening yet treatable cause of metabolic encephalopathy in adults
Publication history
- Accepted June 24, 2014
- First published August 14, 2014.
Online issue publication
February 20, 2018
Article Versions
- Previous version (14 April 2016).
- You are viewing the most recent version of this article.
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions
Other content recommended for you
- Late-onset ornithine transcarbamylase deficiency mimicking a focal opercular syndrome
- Valproate-induced fatal acute hyperammonaemia-related encephalopathy in late-onset ornithine transcarbamylase deficiency
- Ammonia: what adult neurologists need to know
- Coma query cause
- Drug-induced hyperammonaemia
- Unusual cause of general malaise: a young woman with ornithine transcarbamylase deficiency
- Neurological outcome of patients with ornithine carbamoyltransferase deficiency
- Multidisciplinary management of ornithine transcarbamylase (OTC) deficiency in pregnancy: essential to prevent hyperammonemic complications
- Corticosteroid-induced hyperammonaemic encephalopathy in a woman with late-onset ornithine transcarbamylase deficiency
- How to use serum ammonia