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Korean Journal of Medicine ; : 867-872, 1998.
Article Dans Coréen | WPRIM | ID: wpr-170231

Résumé

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.


Sujets)
Adulte , Humains , Mâle , Anévrysme , Tissu conjonctif , Maladie des artères coronaires , Vaisseaux coronaires , Dilatation pathologique , Syndrome d'Ehlers-Danlos , Coeur , Syndrome de Marfan , Prévalence , Syphilis
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