A Case of Noonan Syndrome Presenting with Malignant Hypertension in an Adult / 대한내과학회지
Korean Journal of Medicine
;
: 433-438, 2015.
Article
Dans Coréen
| WPRIM
| ID: wpr-205901
ABSTRACT
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.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Sténose de la valve pulmonaire
/
Occlusion artérielle rénale
/
Cardiomyopathie hypertrophique
/
Valvuloplastie par ballonnet
/
Thorax en entonnoir
/
Cardiopathies congénitales
/
Hypertension artérielle maligne
/
Syndrome de Noonan
Limites du sujet:
Adulte
/
Humains
/
Mâle
langue:
Coréen
Texte intégral:
Korean Journal of Medicine
Année:
2015
Type:
Article
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