Crigler-Najjar syndrome type 1 (Q91602): Difference between revisions
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A síndrome de Crigler-Najjar tipo 1 é a forma mais grave da síndrome de Crigler-Najjar, um distúrbio hereditário da conjugação da bilirrubina hepática, caracterizado por hiperbilirrubinemia neonatal não conjugada grave devido à ausência completa de bilirrubina hepática glucuronosiltransferase. | |||
| description / en | description / en | ||
Crigler-Najjar syndrome type 1 is the most severe form of Crigler-Najjar syndrome, a hereditary disorder of hepatic bilirubin conjugation, characterised by severe neonatal unconjugated hyperbilirubinemia due to a complete absence of hepatic bilirubin glucuronosyltransferase (BGT). | |||
Revision as of 18:37, 15 August 2026
Crigler-Najjar syndrome type 1 is the most severe form of Crigler-Najjar syndrome, a hereditary disorder of hepatic bilirubin conjugation, characterised by severe neonatal unconjugated hyperbilirubinemia due to a complete absence of hepatic bilirubin glucuronosyltransferase (BGT).
| Language | Label | Description | Also known as |
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| default for all languages | ID_1098453659 |
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| English | Crigler-Najjar syndrome type 1 |
Crigler-Najjar syndrome type 1 is the most severe form of Crigler-Najjar syndrome, a hereditary disorder of hepatic bilirubin conjugation, characterised by severe neonatal unconjugated hyperbilirubinemia due to a complete absence of hepatic bilirubin glucuronosyltransferase (BGT). |
