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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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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMJ Publishing Group
2014
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| Matèries: | |
| Accés en línia: | 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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