Management of cardiac aspects in children with Noonan syndrome – results from a European clinical practice survey among paediatric cardiologists

Author:

Wolf Cordula M.ORCID,Zenker Martin,Burkitt-Wright Emma,Edouard Thomas,García-Miñaúr Sixto,Lebl JanORCID,Shaikh GuftarORCID,Tartaglia Marco,Verloes Alain,Östman-Smith Ingegerd

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference50 articles.

1. Hypertrophic cardiomyopathy in noonan syndrome treated by MEK-inhibition;Andelfinger;J. Am. Coll. Cardiol.,2019

2. Growth hormone therapy in Noonan's syndrome: non-cardiomyopathic congenital heart disease does not adversely affect growth improvement;Brown;J. Pediatr. Endocrinol. Metab. : JPEM (J. Pediatr. Endocrinol. Metab.),2002

3. Cardiologic abnormalities in Noonan syndrome - phenotypic diagnosis and echocardiographic assessment of 118 patients;Burch;J. Am. Coll. Cardiol.,1993

4. Cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results;Calcagni;Int. J. Cardiol.,2017

5. [Noonan syndrome: genetic and clinical update and treatment options];Carcavilla;Anales de pediatria (Barcelona, Spain : 2003),2020

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