Progressive familial intrahepatic cholestasis type 4: a case report
Abstract Background Progressive familial intrahepatic cholestasis is an autosomal recessive genetic disorder that manifests primarily with jaundice and pruritus and can progresses from persistent cholestasis to cirrhosis and late childhood liver failure. Classically, progressive familial intrahepati...
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| Hlavní autoři: | , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMC
2024-09-01
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| Edice: | Journal of Medical Case Reports |
| Témata: | |
| On-line přístup: | https://doi.org/10.1186/s13256-024-04662-5 |
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