Acute neonatal citrullinaemia type 1 (Q102719): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (One intermediate revision by the same user not shown) | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 19:55, 16 August 2026
Acute neonatal citrullinemia type 1 is a severe form of citrullinemia type 1 characterised clinically by hyperammonemia, progressive lethargy, poor feeding and vomiting, seizures and possible loss of consciousness, within one to a few days of birth, with variable signs of increased intracranial pressure. The condition can lead to significant neurologic deficits.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1802140935 |
||
| English | Acute neonatal citrullinaemia type 1 |
Acute neonatal citrullinemia type 1 is a severe form of citrullinemia type 1 characterised clinically by hyperammonemia, progressive lethargy, poor feeding and vomiting, seizures and possible loss of consciousness, within one to a few days of birth, with variable signs of increased intracranial pressure. The condition can lead to significant neurologic deficits. |
Statements
CID11:ID_1802140935
0 references
dki-india-ID_1802140935
0 references
Concluído
0 references
15 August 2026
0 references
