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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...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Iuliu Hatieganu University of Medicine and Pharmacy
2021
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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 |
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author | Tcaciuc, Eugen Podurean, Mariana Tcaciuc, Angela |
author_facet | Tcaciuc, Eugen Podurean, Mariana Tcaciuc, Angela |
author_sort | Tcaciuc, Eugen |
collection | PubMed |
description | 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 encephalopathy that can result in permanent neurologic sequelae. Type 2 disease is associated with a lower serum bilirubin concentration and affected patients survive into adulthood without neurologic impairment. Currently, liver transplantation is the only available therapeutic method for these patients. Developing new curative approaches is a clinical need. |
format | Online Article Text |
id | pubmed-8411811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Iuliu Hatieganu University of Medicine and Pharmacy |
record_format | MEDLINE/PubMed |
spelling | pubmed-84118112021-09-14 Management of Crigler-Najjar syndrome Tcaciuc, Eugen Podurean, Mariana Tcaciuc, Angela Med Pharm Rep Articles 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 encephalopathy that can result in permanent neurologic sequelae. Type 2 disease is associated with a lower serum bilirubin concentration and affected patients survive into adulthood without neurologic impairment. Currently, liver transplantation is the only available therapeutic method for these patients. Developing new curative approaches is a clinical need. Iuliu Hatieganu University of Medicine and Pharmacy 2021-08 2021-08-10 /pmc/articles/PMC8411811/ /pubmed/34527915 http://dx.doi.org/10.15386/mpr-2234 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License |
spellingShingle | Articles Tcaciuc, Eugen Podurean, Mariana Tcaciuc, Angela Management of Crigler-Najjar syndrome |
title | Management of Crigler-Najjar syndrome |
title_full | Management of Crigler-Najjar syndrome |
title_fullStr | Management of Crigler-Najjar syndrome |
title_full_unstemmed | Management of Crigler-Najjar syndrome |
title_short | Management of Crigler-Najjar syndrome |
title_sort | management of crigler-najjar syndrome |
topic | Articles |
url | 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 |
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