Cargando…
Management of Crigler-Najjar syndrome
Crigler-Najjar syndrome is a rare autosomal recessive inherited non-hemolytic unconjugated hyperbilirubinemia caused by UDP-glucuronosyltransferase deficiency. There are two forms of this disorder. Type 1 disease is associated with severe jaundice and neurologic impairment due to bilirubin encephalo...
Autores principales: | Tcaciuc, Eugen, Podurean, Mariana, Tcaciuc, Angela |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Iuliu Hatieganu University of Medicine and Pharmacy
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8411811/ https://www.ncbi.nlm.nih.gov/pubmed/34527915 http://dx.doi.org/10.15386/mpr-2234 |
Ejemplares similares
-
Perioperative management of a patient with hemophilia A and crigler-najjar syndrome
por: Bhoi, Debesh, et al.
Publicado: (2013) -
A Rare Case Report of Crigler Najjar Syndrome Type II
por: Abdul Raffay, Eusha, et al.
Publicado: (2021) -
Crigler-Najjar syndrome type 2: Novel UGT1A1 mutation
por: Nair, Karippoth Mohandas, et al.
Publicado: (2012) -
p.Cys223Tyr mutation causing Crigler–Najjar syndrome type II
por: Xiong, Qing‐Fang, et al.
Publicado: (2020) -
Perioperative Management of Patient with Esophageal Carcinoma and Crigler-Najjar Syndrome Type 2: A Case Report
por: Ma, Dehua, et al.
Publicado: (2022)