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Korean Journal of Medicine ; : 433-438, 2015.
Artículo en Coreano | WPRIM | ID: wpr-205901

RESUMEN

Noonan syndrome is an autosomal dominant disorder characterized by dysmorphic facial features, congenital heart defects and short stature. To date, renal artery stenosis has not been associated with Noonan syndrome. We report the case of a 27-year old male who presented with malignant hypertension associated with renal artery stenosis, dysmorphic facial features, pectus excavatum, pulmonary stenosis and hypertrophic cardiomyopathy who was diagnosed with Noonan syndrome.


Asunto(s)
Adulto , Humanos , Masculino , Valvuloplastia con Balón , Cardiomiopatía Hipertrófica , Tórax en Embudo , Cardiopatías Congénitas , Hipertensión Maligna , Síndrome de Noonan , Estenosis de la Válvula Pulmonar , Obstrucción de la Arteria Renal
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