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Korean Journal of Medicine ; : 867-872, 1998.
Artículo en Coreano | WPRIM | ID: wpr-170231

RESUMEN

Marfan's syndrome is a an autosomal dominant disorder of connective tissue that is characterized by ocular, skeletal, and cardiovascular manifestation. It is estimated to have a prevalence of 4-6 per 10,000 people, and at least 25 percent of the cases occur in the absence of a family history. Coronary artery ectasia is a diffuse abnormality of the vessel wall, which has been reported in associated with coronary atherosclerosis, infectious process, congenital heart lesion, syphilis, Ehlers-Danlos syndrome. We reported a case of 25-year-old male who presented with Marfan's syndrome associated with dissecting ascending arotic aneurysm and diffuse dilatated coronary artery ectasia. Coronary angiographic study demonstrated the diffusely dilatated coronary artery ectasia.


Asunto(s)
Adulto , Humanos , Masculino , Aneurisma , Tejido Conectivo , Enfermedad de la Arteria Coronaria , Vasos Coronarios , Dilatación Patológica , Síndrome de Ehlers-Danlos , Corazón , Síndrome de Marfan , Prevalencia , Sífilis
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