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  • Inkontinenca pigmenta : klinične in genetske značilnosti = Incontinentia pigmenti : clinical and genetic aspect
    Peterlin, Borut, 1963- ; Podrumac, Božena ; Stirn-Kranjc, Branka
    Incontinentia pigmenti (IP) is an X linked dominant disorder with a prevalenceof about 1 in 38 000. Clinical diagnosis is based on the characteristic evolution of skin lesions (particularly stages I ... and III), ectodermally derived tissues (especially teeth) as well as family history of disease. Indirect molecular genetic diagnosis is possible in familial cases due to localisation of the IP II gene in the Xq28 region.
    Vir: Slovenska pediatrija : revija Združenja pediatrov Slovenije in Združenja specialistov šolske in visokošolske medicine Slovenije. - ISSN 1318-4423 (Letn. 7, suppl. 1, 2000, str. 120-121)
    Vrsta gradiva - članek, sestavni del
    Leto - 2000
    Jezik - slovenski
    COBISS.SI-ID - 11342041

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