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  • Title: Multiple lentigines syndrome in a Nigerian family.
    Author: Kubeyinje EP, Onunu AN, Obasohan AO.
    Journal: Trop Geogr Med; 1993; 45(3):135-7. PubMed ID: 8362457.
    Abstract:
    Three cases of the multiple lentigines syndrome are reported in a Nigerian family, involving a father and two of his children. The major abnormalities in this syndrome include: multiple lentigines, cardiac defects, genitourinary malformations, neurological deficits, growth retardation, cephalofacial dysmorphism and a family history consistent with an autosomal dominant mode of inheritance. We hereby report these cases in whom the main features are multiple lentigines, ocular hypertelorism, electrocardiographic defects and a pattern consistent with an autosomal dominant mode of inheritance.
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