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Korean Journal of Anesthesiology ; : 371-375, 2009.
Artículo en Coreano | WPRIM | ID: wpr-189216

RESUMEN

Loeys-Dietz Syndrome (LDS) is a recently described autosomal dominant aortic aneurysm syndrome with widespread systemic involvement. It is characterized by the triad of 1) arterial tortuosity and aneurysms, 2) hypertelorism, and 3) bifid uvula or cleft palate. A 12-year-old boy with LDS was scheduled to undergo correction of aortic valve regurgitation due to aortic annuloectasia. We report our clinical experiences of a case of LDS patient with brief review of related literatures and relevant anesthetic problems.


Asunto(s)
Niño , Humanos , Aneurisma , Aneurisma de la Aorta , Válvula Aórtica , Arterias , Fisura del Paladar , Hipertelorismo , Inestabilidad de la Articulación , Síndrome de Loeys-Dietz , Enfermedades Cutáneas Genéticas , Úvula , Malformaciones Vasculares
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