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...

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Detalles Bibliográficos
Autores principales: Pati, Girish Kumar, Singh, Ayaskanta, Nath, Preetam, Narayan, Jimmy, Padhi, Pradeep Kumar, Parida, Prasanta Kumar, Pattnaik, Kaumudee, Panda, Chittaranjan, Singh, Shivaram Prasad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134282/
https://www.ncbi.nlm.nih.gov/pubmed/27906097
http://dx.doi.org/10.1186/s13256-016-1126-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134282/
https://www.ncbi.nlm.nih.gov/pubmed/27906097
http://dx.doi.org/10.1186/s13256-016-1126-x

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