LEOPARD syndrome


LEOPARD syn·drome

[MIM*151100] syndrome consisting of lentigines (multiple), electrocardiographic abnormalities, ocular hypertelorism, pulmonary stenosis, abnormalities of genitalia, retardation of growth, and deafness (sensorineural). An autosomal dominant hereditary disorder. Synonym(s): multiple lentigines syndrome
An autosomal dominant [MIM 151100] condition with thousands of 1–5-mm darkly pigmented macules on the skin

leopard syndrome

Multiple lentigines syndrome An AD condition with thousands of 1-5 mm darkly pigmented macules on the skin, not mucosae Clinical characterized by the acronym LEOPARD–Lentigines, EKG disturbances, Ocular hypertelorism, Pulmonary stenosis, Abnormalities of genitalia–gonadal or ovarian hypoplasia, Retarded growth, neural Deafness

LEOPARD syn·drome

(lep'ărd sin'drōm) A hereditary syndrome consisting of lentigines (multiple), electrocardiographic abnormalities, ocular hypertelorism, pulmonary stenosis, abnormalities of genitalia, retardation of growth, and deafness (sensorineural).

LEOPARD syn·drome

(lep'ărd sin'drōm) [MIM*151100] Syndrome consisting of lentigines (multiple), electrocardiographic abnormalities, ocular hypertelorism, pulmonary stenosis, abnormalities of genitalia, retardation of growth, and deafness (sensorineural).