Marfan syndrome. Report of a patient
Marfan syndrome is a congenital hereditary disease (sporadic in 15-30% of cases) of connective tissue, dominant autosomal with complete penetrance, with prevalence estimated at one per 5 000 people and incidence of one per 10 000 births without racial or sex predominance. A patient with sporadic Mar...
| Príomhchruthaitheoirí: | , , |
|---|---|
| Formáid: | Alt |
| Teanga: | Spanish |
| Foilsithe / Cruthaithe: |
Editorial Ciencias Médicas
2015-12-01
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| Sraith: | Acta Médica del Centro |
| Ábhair: | |
| Rochtain ar líne: | http://www.revactamedicacentro.sld.cu/index.php/amc/article/view/292 |