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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...
Autores principales: | Bhende, Vishal V, Majmudar, Hardil P, Sharma, Tanishq S, Pathan, Sohilkhan R, Mehta, Deepakkumar V |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2021
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Materias: | |
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 |
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