Alagille syndrome associated with total anomalous pulmonary venous connection and severe xanthomas: A case report

BACKGROUND: Alagille syndrome (ALGS) is an autosomal dominant genetic disorder caused by mutations in the JAG1 or NOTCH2 gene. It is characterized by decreased intrahepatic bile ducts associated with a variety of abnormalities in many other organ systems, such as the cardiovascular, skeletal, and ur...

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Detalles Bibliográficos
Autores principales: Zeng, Han-Shi, Zhang, Zhan-Hui, Hu, Yan, Zheng, Gui-Lang, Wang, Jing, Zhang, Jing-Wen, Guo, Yu-Xiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477039/
https://www.ncbi.nlm.nih.gov/pubmed/36157644
http://dx.doi.org/10.12998/wjcc.v10.i25.8932

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477039/
https://www.ncbi.nlm.nih.gov/pubmed/36157644
http://dx.doi.org/10.12998/wjcc.v10.i25.8932

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