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Crigler Najjar Syndrome Type 2 (CNS Type 2): An Unwonted Cause of Jaundice in Adults
Crigler Najjar Syndrome (CNS) Type 2 is an uncommon genetic disorder characterised by non-haemolytic unconjugated hyperbilirubinemia. It is caused by mutations in the UGT1A1 gene which codes for the enzyme uridine diphosphate glucoronosyl transferase- 1, required for the conjugation and further excr...
שמור ב:
| הוצא לאור ב: | J Clin Diagn Res |
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| Main Authors: | , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
JCDR Research and Publications (P) Limited
2017
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5583863/ https://ncbi.nlm.nih.gov/pubmed/28892962 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7860/JCDR/2017/28195.10221 |
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