Article

Ventricular arrhythmia and Noonan Syndrome with LZTR1 Mutations: Expanding the Phenotype with a Case Report and Review of the Literature

2024-03-27

Abstract excerpt

<h4>Background: </h4> Noonan syndrome (NS) is characterized by typical facial features, short stature, congenital heart defects and other comorbidities, which is caused by germline mutations in genes coding for components of the Ras-mitogen-activated protein kinase (RAS-MAPK) pathway. Noonan syndrome is an inherited disease involving multiple systems, but ventricular arrhythmia in Noonan syndrome is rarely reporte...

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Literature Corpus work: 6037f4c3-21f3-5879-8dc9-835b975b0a6a
DOI: 10.21203/rs.3.rs-4122815/v1

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