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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Hindawi Publishing Corporation
2017
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| 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 |