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A Rare Case Report of Crigler Najjar Syndrome Type II
Crigler-Najjar syndrome is an inborn error of metabolism caused by a point mutation in one of the five exons of UGT1A1 gene, the product of which is responsible for elimination of bilirubin via bile. A number of hyperbilirubinemia disorders similar to Crigler-Najjar syndrome are reported, but they d...
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| Udgivet i: | Cureus |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Cureus
2021
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7880822/ https://ncbi.nlm.nih.gov/pubmed/33604208 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.12669 |
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