A Case of Infantile Alagille Syndrome With Severe Dyslipidemia: New Insight into Lipid Metabolism and Therapeutics

Alagille syndrome (AGS) is an autosomal dominant genetic disorder characterized by congenital heart disease, hepatic cholestasis, dyslipidemia, and characteristic facies since infancy. Cholestatic hypercholesterolemia in patients diagnosed with AGS is occasionally refractory and resistant to convent...

Descripción completa

Detalles Bibliográficos
Autores principales: Nakajima, Hisakazu, Tsuma, Yusuke, Fukuhara, Shota, Kodo, Kazuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8826833/
https://www.ncbi.nlm.nih.gov/pubmed/35155971
http://dx.doi.org/10.1210/jendso/bvac005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8826833/
https://www.ncbi.nlm.nih.gov/pubmed/35155971
http://dx.doi.org/10.1210/jendso/bvac005

Ejemplares similares