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Benign recurrent intrahepatic cholestasis type 2 in a child: A case report and novel mutation
Benign recurrent intrahepatic cholestasis is a rare disorder characterized by recurrent episodes of cholestatic jaundice without liver damage. A mutation in the ABCB11 gene encoding bile salt export pump protein causes the disease. A 16-year-old boy with severe jaundice is presented here. His labora...
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| Yayımlandı: | Turk Arch Pediatr |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Turkish Pediatric Association
2021
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8114600/ https://ncbi.nlm.nih.gov/pubmed/34013234 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14744/TurkPediatriArs.2020.74507 |
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