Noonan syndrome with multiple lentigines
Noonan syndrome with multiple lentigines
Definition
A rare multisystem genetic disorder characterized by lentigines, hypertrophic cardiomyopathy, short stature, pectus deformity, and dysmorphic facial features.
Also known as Cardiomyopathic lentiginosis, familial multiple lentigines syndrome, generalised lentiginosis, lentigines, electrocardiographic conduction defects, 0cular hypertelorism, pulmonary stenosis, abnormalities of the genitals, retarded Growth, deafness, LEOPARD syndrome, Noonan syndrome with multiple lentigines — per MONDO