Citrullinaemia type 1 (Q88501): Difference between revisions
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Latest revision as of 14:44, 15 August 2026
Citrullinemia type 1 is a rare autosomal recessive urea cycle defect characterised clinically by hyperammonemia, progressive lethargy, poor feeding and vomiting in the neonatal form (Acute neonatal citrullinemia type 1, ) and by variable hyperammonemia in the later-onset form (Adult-onset citrullinemia type 1, ).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1410274578 |
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| English | Citrullinaemia type 1 |
Citrullinemia type 1 is a rare autosomal recessive urea cycle defect characterised clinically by hyperammonemia, progressive lethargy, poor feeding and vomiting in the neonatal form (Acute neonatal citrullinemia type 1, ) and by variable hyperammonemia in the later-onset form (Adult-onset citrullinemia type 1, ). |
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CID11:ID_1410274578
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dki-india-ID_1410274578
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Concluído
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13 August 2026
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