Singleton Merten Syndrome: A Rare Cause of Early Onset Aortic Stenosis

Singleton Merten syndrome (SMS) is a rare autosomal dominant genetic disorder with variable expression. Its characteristic features include abnormal aortic calcification, abnormal ossification of extremities, and dental anomalies. We present a young man with dyspnea who was noted to have aortic sten...

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Detalles Bibliográficos
Autores principales: Ghadiam, Harshavardhan, Mungee, Sudhir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339492/
https://www.ncbi.nlm.nih.gov/pubmed/28321341
http://dx.doi.org/10.1155/2017/8197954

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339492/
https://www.ncbi.nlm.nih.gov/pubmed/28321341
http://dx.doi.org/10.1155/2017/8197954

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