Clinical, pathological and dermoscopic characteristics of cutaneous lesions in LEOPARD syndrome

LEOPARD syndrome (LS) is a rare autosomal disorder associated with multiple congenital anomalies. This term is an acronym for Lentigines (LT), Electrocardiographic conduction defects, Ocular hypertelorism, Pulmonary valve stenosis, Abnormalities of the genitalia, Retardation of growth, and Deafness ^1-3. Mutations in PTPN11 gene cause this syndrome in around 90% of cases, and less frequently other mutations produce this entity^3-4.

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