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Cardiol Young ; 10(6): 582-9, 2000 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11117390

RESUMO

We describe what is, to the best of our knowledge, a previously unreported association in patients with similar facial features, skin and joint laxity, of lengthening and tortuosity of systemic, pulmonary and coronary vessels. We evaluated 12 patients with similar phenotypes, from eight different families. Detailed echocardiographic and angiographic evaluations were performed in all, and biopsies of the skin in seven. All patients have elongated facies, prominent ears, micrognathia and laxity of their joints. Angiographic pictures showed a varying degree of lengthening and tortuosity of systemic, pulmonary, and coronary arteries. Pulsatile carotid arteries formed cervical masses in 2 patients, and three had severe renal arterial stenoses. All showed varying degrees of branch and peripheral pulmonary arterial stenosis, necessitating placement of stents in six. Biopsy of the skin proved normal in all seven patients studied, thus excluding cutis laxa, Ehlers-Danlos and Marfan syndromes. The constellation of abnormalities suggests a genetic syndrome of connective tissue etiology. Further genetic studies, and gene mapping, are underway.


Assuntos
Doenças da Aorta/diagnóstico , Doença das Coronárias/diagnóstico , Face/anormalidades , Artéria Pulmonar , Doenças Vasculares/diagnóstico , Adolescente , Adulto , Doenças da Aorta/genética , Criança , Pré-Escolar , Consanguinidade , Doença das Coronárias/genética , Saúde da Família , Feminino , Humanos , Masculino , Fenótipo , Síndrome , Anormalidade Torcional , Doenças Vasculares/genética
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