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  • Sindrom Di George = Di George syndrome
    Bratina, Petra, 1982- ...
    We describe a case of a newborn with DiGeorge Syndrome, classically defined asa congenital T-cell immunodeficiency, which is characterised by conotruncal cardiac anomalies, unusual facies, ... hypoplastic thymus and hypocalcaemic tetany. Many, but not all, patients with DiGeorge Syndrome have a heterozygousdeletion of chromosome 22, which is one of the most common chromosomal abnormalities known.
    Vir: Slovenska pediatrija : revija Združenja pediatrov Slovenije in Združenja specialistov šolske in visokošolske medicine Slovenije. - ISSN 1318-4423 (Letn. 13, št. 4, 2006, str. 217-222)
    Vrsta gradiva - članek, sestavni del
    Leto - 2006
    Jezik - slovenski
    COBISS.SI-ID - 22429401

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