Marfan Syndrome: Regarding Two Cases
Marfan syndrome is an autosomal dominant genetic disorder, with a prevalence of 1 every 5,000-10,000 newborns, so it is classified as an uncommon disease. It affects multiple organs and systems; its prognosis is marked by the cardiovascular involvement. Multidisciplinary follow-up of these patients...
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| Autori principali: | , , |
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| Natura: | Artigo |
| Lingua: | Espanhol |
| Pubblicazione: |
Universidad de las Ciencias Médicas de Cienfuegos
2020-02-01
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| Serie: | Revista Finlay |
| Soggetti: | |
| Accesso online: | https://revfinlay.sld.cu/index.php/finlay/article/view/793 |
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