Case report: Crigler-Najjar syndrome type 1 in Croatia—more than a one in a million: a case series

Crigler-Najjar syndrome (CNS) is an exceedingly rare autosomal recessive disease with an estimated incidence of 1 in a million live births. CNS type 1 (CNS1) is the most severe form, characterized by severe unconjugated hyperbilirubinemia since birth due to the absence of hepatic uridine 5'-dip...

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Detalles Bibliográficos
Autores principales: Kovačić Perica, Matea, Todorić, Ivana, Marčinković, Nedo, Džepina, Petra, Aničić, Mirna Natalija, Mrzljak, Anna, Vuković, Jurica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620791/
https://www.ncbi.nlm.nih.gov/pubmed/37928349
http://dx.doi.org/10.3389/fped.2023.1276349

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620791/
https://www.ncbi.nlm.nih.gov/pubmed/37928349
http://dx.doi.org/10.3389/fped.2023.1276349

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