Nonhepatic Alagille Syndrome Associated With Predominant Cardioskeletal Anomalies: A Rare Case

Alagille syndrome (ALGS) is a rare autosomal dominant genetic disorder with multisystem involvement including the liver, heart, skeleton, eyes, kidneys, and other organ systems, along with characteristic facial abnormalities. Some patients with ALGS may have isolated involvement of a particular syst...

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Detalles Bibliográficos
Autores principales: Bhende, Vishal V, Majmudar, Hardil P, Sharma, Tanishq S, Pathan, Sohilkhan R, Mehta, Deepakkumar V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Cardiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8460555/
https://www.ncbi.nlm.nih.gov/pubmed/34589338
http://dx.doi.org/10.7759/cureus.17429

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8460555/
https://www.ncbi.nlm.nih.gov/pubmed/34589338
http://dx.doi.org/10.7759/cureus.17429

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