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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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Hlavní autoři: Ozyuksel, Arda, Ersoy, Cihangir, Canturk, Emir, Akcevin, Atif
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Publishing Group 2014
Témata:
On-line přístup: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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