Corticosteroid-induced hyperammonaemic encephalopathy in a woman with late-onset ornithine transcarbamylase deficiency
- PMID: 38697679
- PMCID: PMC11085957
- DOI: 10.1136/bcr-2023-255793
Corticosteroid-induced hyperammonaemic encephalopathy in a woman with late-onset ornithine transcarbamylase deficiency
Abstract
Ornithine transcarbamylase deficiency (OTCD) is a rare, X linked disorder that can manifest in late adulthood in heterozygous females as severe hyperammonaemia following environmental stressors. We present a case of hyperammonaemic encephalopathy that was triggered by glucocorticoid administration in an adult woman with heterozygous OTCD with clinical response to haemodialysis, ammonia scavengers and a high-calorie, low-protein diet.
Keywords: Dialysis; Genetics; Medical management; Unwanted effects / adverse reactions.
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Conflict of interest statement
Competing interests: None declared.
References
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- Lichter-Konecki U, Caldovic L, Morizono H, et al. Ornithine Transcarbamylase deficiency. In: Adam MP, Ardinger HH, Pagon RA, et al., eds. PubMed. Seattle (WA): University of Washington, Seattle, 1993. - PubMed
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