Metadata
Author: Common crawl
Data
English[en]
Marfan’s syndrome is an autosomal dominant disorder of connective tissue due to the abnormal expression of fibrillin 1 and characterized by manifestations in the cardiovascular, musculoskeletal and ophtalmic systems. Cutaneous manifestations are minor findings and include striae atrophicae, skin hyperextensibility and joint laxity.
Spanish[es]
Enfermedad hereditaria del tejido conectivo que se caracteriza por una estatura alta, extremidades alargadas, subluxación del cristalino, dilatación de la aorta ascendente, anomalías craneofaciales y pectus carinatum.