Japanese Circulation Journal · 2001 · 13 citations · 22 references
MedicineCardiologyPediatricsCardiovascular GeneticsClinical CardiologyPediatric CardiologyCardiovascular DiseaseCongenital Heart DiseaseCongenital Heart Disease GeneticsHypertrophic Cardiomyopathy GeneticsInherited CardiomyopathiesValvular Heart DiseaseAdrenergic Receptor AgonistsAdrenergic Receptor AntagonistsAdrenergic Receptor SignalingClinicopathological CorrelationGenetic Linkage AnalysisPulmonary Valve StenosisRight Ventricular Outflow Tract ObstructionSyndromic Cardiomyopathy
This report describes an adult patient with Noonan syndrome accompanied by biventricular hypertrophic cardiomyopathy causing isolated right ventricular outflow tract obstruction. Biventricular hypertrophic cardiomyopathy causing right- and/or left-side outflow tract obstruction, as well as valvular pulmonary stenosis, is relatively common in infants with Noonan syndrome. However, this condition without a dysplastic pulmonary valve, or indeed any polyvalvular dysplasia, is rare in adults with Noonan syndrome. Treatment with a beta-adrenergic receptor blocking agent improved the patient's symptoms. Because neither the etiologic and prognostic relationship nor the genetic linkage between hypertrophic cardiomyopathy associated with Noonan syndrome and non-syndromic hypertrophic cardiomyopathy is clearly defined, clinicopathological findings and further follow-up may provide important evidence for the pathogenesis of hypertrophic cardiomyopathy.
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A clinical study of Noonan syndrome.
Mike Sharland, Michael Burch, W M McKenna et al. · Archives of Disease in Childhood · 1992 · 477 citations · Full text
Medicine, Cardiology, Pediatrics +13
Mapping a gene for Noonan syndrome to the long arm of chromosome 12
C. Ruth Jamieson, Ineke van der Burgt, Angela F. Brady et al. · Nature Genetics · 1994 · 290 citations