Valproate-induced hyperammonemia - uncovering an underlying inherited metabolic disorder: a case report
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://link.springer.com/content/pdf/10.1186/s13256-018-1666-3.pdf
Reference6 articles.
1. Tarafdar S, Slee M, Ameer F, et al. A case of valproate induced hyperammonaemic encephalopathy. Case Rep Med. 2011;(2):969505.
2. Oechsner M, Steen C, Sturenburg HJ, et al. Hyperammonaemic encephalopathy after initiation of valproate therapy in unrecognised ornithine transcarbamylase deficiency. J Neurol Neurosurg Psychiatry. 1998;64:680–2.
3. Choi DA, Lee KW, Shin YT, Na KR. Hyperammonemia in a patient with late-onset ornithine carbamoyltransferase deficiency. J Korean Med Sci. 2012;27:556–9.
4. Tuchman M, Morizono H, Rajagopal BS, et al. The biochemical and molecular spectrum of ornithine transcarbamylase deficiency. J Inherit Metab Dis. 1998;21:40–58.
5. Klein OD, Kostiner DR, Weisiger K, et al. Acute fatal presentation of ornithine transcarbamylase deficiency in a previously healthy male. Hepatol Int. 2008;2:390–4.
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