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KMID : 0032220110230020232
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Annals of Dermatology
2011 Volume.23 No. 2 p.232 ~ p.235
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LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD
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Kim Ji-Hyun
Kim Mi-Ri
Kim Hee-Jung
Lee Kyung-A
Lee Min-Geol
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Abstract
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LEOPARD multiple congenital anomaly syndrome inherited in an autosomal dominant manner. LEOPARD is an acronym for Lentigines, Eletrocardiographic conduction defects, Ocular hypertelorism, Pulmonary valve stenosis, Abnormalities of the genitalia, Retardation of growth, and Deafness. Clinical diagnosis is primarily based on multiple lentigines, typical facial features, and the presence of hypertrophic cardiomyopathy and/or cafe-au-lait macules. We report a typical case of LEOPARD syndrome with PTPN11 gene mutation associated with lentigines, electrocardiograph abnormality, ocular hypertelorism, pulmonary valve stenosis, growth retardation, and sensorineural hearing loss.
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KEYWORD
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LEOPARD syndrome, Multiple lentigines, PTPN11 gene
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