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Argininosuccinic aciduria
rareArgininosuccinic aciduria (ASA) is a disorder of urea cycle metabolism most commonly characterized by either a severe, neonatal-onset form that manifests with hyperammonemia accompanied with vomiting, hypothermia, lethargy and poor feeding in the first few days of life, or late-onset forms (any age outside the newborn period) that manifest with stress or infection-induced episodic hyperammonemia or, in some, behavioral abnormalities and/or learning disabilities. Patients often manifest liver dysfunction.
- Identifiers
- MONDO:0008815 OMIM:207900Orphanet:23
- Causal genes
- ASL
- Also known as
- arginino succinase deficiency · argininosuccinase deficiency · argininosuccinate acidemia · argininosuccinatelyase deficiency · argininosuccinic acid lyase deficiency
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