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Progressive supra-aortic stenosis in a young adult with the findings of Singleton Merten Syndrome
Singleton Merten Syndrome is an autosomal dominant disorder of unknown origin. Patients often present with muscular weakness, failure to thrive, abnormal dentition, glaucoma, psoriatic skin lesions, aortic calcification and musculoskeletal abnormalities. In this case, we present a young girl with a...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4158224/ https://ncbi.nlm.nih.gov/pubmed/25193816 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2014-205985 |
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