Noonan syndrome with multiple lentigines

A rare multisystem genetic disorder characterized by lentigines, hypertrophic cardiomyopathy, short stature, pectus deformity, and dysmorphic facial features.

Also known as: Cardiomyopathic lentiginosis, LEOPARD syndrome, Noonan syndrome with multiple lentigines, familial multiple lentigines syndrome, generalised lentiginosis, lentigines, electrocardiographic conduction defects, 0cular hypertelorism, pulmonary stenosis, abnormalities of the genitals, retarded Growth, deafness, Moynahan syndrome, lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonic stenosis, abnormal genitalia, retardation of growth, Deafnes

14 clinical trials for this condition and its sub-types, 3 tagged with Noonan syndrome with multiple lentigines itself.