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  • Reyev sindrom in bolezni s podobnim kliničnim potekom = Reye syndrome and "Reye like" diseases
    Rus, Rina ...
    We report a case of a 4-years-old boy; who presented with typical clinical manifestations of Reye syndrome. Laboratorial findings suggested the medium chain acyl CoA dehidrogenase deficiency (MCAp) ... that is an inherited defect of mitochondrial beta oxydation. Epidemiology, clinical picture, differential diagnosis and therapy of Reye syndrome and Reye like diseases such as MCAD arepresented.
    Type of material - article, component part
    Publish date - 2000
    Language - slovenian
    COBISS.SI-ID - 13512921