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A 10-year-old child presenting with syndromic paucity of bile ducts (Alagille syndrome): a case report
BACKGROUND: Alagille syndrome, a rare genetic disorder with autosomal dominant transmission, manifests with five major features: paucity of interlobular bile ducts, characteristic facies, posterior embryotoxon, vertebral defects, and peripheral pulmonary stenosis. Globally, only 500 cases have so fa...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | J Med Case Rep |
|---|---|
| Prif Awduron: | , , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
BioMed Central
2016
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5134282/ https://ncbi.nlm.nih.gov/pubmed/27906097 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-016-1126-x |
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