The American journal of emergency medicine
July 6, 2026 · via Europe PMC
Unexplained hyperammonemia in the emergency department: Late-onset ornithine transcarbamylase deficiency in a 75-year-old man.
Lee JH, Moon S, Jung H, Kim YJ, Ahn JY.
AI summary — for doctors, generated from the abstract only
This case of late-onset ornithine transcarbamylase deficiency in a 75-year-old with hyperammonemic coma shows urea cycle disorders can present in older adults.
What was studied
A case report of a 75-year-old man with acute confusion, vomiting, and coma with unexplained hyperammonemia (peak 487 µmol/L).
Key findings
- Deteriorated despite lactulose; required intubation and emergent hemodialysis.
- Family history: two nephews died of unexplained hyperammonemia.
- Elevated ornithine, low citrulline; hemizygous OTC variant confirmed.
- Treated with hemodialysis, IV L-arginine, and protein restriction; discharged without focal deficits.
Clinical relevance
This raises awareness to consider urea cycle disorders in unexplained hyperammonemia at any age and supports early hemodialysis before genetic confirmation.
Who should care
Limitations
Single case report.
Unexplained high ammonia in an older adult without liver disease? Consider a urea cycle disorder.
This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates — verify against the original source before acting on it.
Abstract
Late-onset ornithine transcarbamylase deficiency (OTCD) is an extremely rare X-linked urea cycle disorder in the geriatric population, and its diagnosis in the emergency department (ED) is highly challenging. We report the case of a 75-year-old man who presented to the ED with acute confusion and vomiting that rapidly progressed to coma. Initial investigations revealed unexplained hyperammonemia. Despite an empiric lactulose enema, his neurological status continued to deteriorate, and his plasma ammonia level peaked at 487 μmol/L. He required endotracheal intubation, and emergent hemodialysis was initiated. A detailed family history revealed that two nephews had died from unexplained hyperammonemia, raising a high index of suspicion for an inherited metabolic disorder. Subsequent plasma amino acid analysis revealed elevated ornithine and decreased citrulline levels. The diagnosis was confirmed by next-generation sequencing, which identified a hemizygous OTC variant (c.119G > A, p.Arg40His). The patient was successfully managed with hemodialysis, intravenous L-arginine, and a protein-restricted diet, and he was ultimately discharged without focal neurological sequelae. This case highlights that clinicians should consider urea cycle disorders in the differential diagnosis of unexplained hyperammonemia regardless of age, including in geriatric patients. Furthermore, it underscores the critical value of a comprehensive family history and the prompt initiation of hemodialysis-before genetic confirmation-to prevent irreversible neurological damage in atypical adult presentations.
DOI
10.1016/j.ajem.2026.07.008
PMID
42442071
Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.
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