Case reportMultiple lentigines syndrome: Case report and review of the literature
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Cited by (181)
A rare mutation in a patient with Noonan syndrome with multiple lentigines
2023, JAAD Case ReportsLEPOARD syndrome: A report of a case with a novel PTPN11 mutation
2021, JAAD Case ReportsFamilial LEOPARD Syndrome With Hypertrophic Cardiomyopathy
2020, American Journal of CardiologyCitation Excerpt :Electrocardiograms of the son (proband) and daughter are presented in Figures 4 and 5; findings are presented in Table 1. Diagnostic criteria for LEOPARD syndrome were proposed by Voron et al in 1976 and include lentigines and 2 other recognized features of LEOPARD syndrome or a first-degree relative with lentigines and 3 other features in the patient.4 Typically, multiple lentigines appear during childhood and expand in number until puberty.5
An incomplete LEOPARD syndrome presented with generalized lentigines
2024, Journal of Cosmetic Dermatology
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From the Dermatology and Endocrine-Metabolic Sections of the Department of Medicine, The Medical College of Wisconsin, Milwaukee, Wisconsin.
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