Population
Patients with Noonan syndrome
Design
Review
Authors
Loading...
Supports clinical recognition of Noonan syndrome; leaves open refinement via contemporary genetic cohorts.
Noonan syndrome is a genetic disorder characterized by congenital heart defects, short stature, and distinct facial features, with an estimated incidence of 1 in 1000 to 1 in 2500 live births.
Judith Allanson (1987) studied this question.
Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context: