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  • Sindrom opsoklonus-mioklonus-ataksija = Opsoclonus-myoclonus-ataxia syndrome
    Špegel, Milan ; Kopač, Štefan
    Background. Opsoclonus-myoclonus-ataxia syndrome (OMAS) is observed mostly in children under3 years of age. Incidence is not known. The leading clinical sings areČ opsoclonus, myoclonus and ataxiač ... only two signs may bepresent. Thesyndrome may follow an infectious disease usually of viral origin, but may be paraneoplastic, associated with a neuroblastoma. The course is ojten prolonged with recurrences but gradual and stepwise improvement. The majority of affected children are left with mental retardation, motorandž orspeech disturbances. There are no known criteria to predict prognosis. Corticosteroidor corticotropin are recommended treatment regimes. Conclusions.The boy with OMAS is described. The diagnosis was made in retrospect. He was not treated, however inspite of thisfacthe has only mild mental retardation and tremorof the hands. He also developed epileptic fits which responded to antiepileptic treatment.
    Vir: Zdravniški vestnik : glasilo Slovenskega zdravniškega društva = Slovenian medical journal = journal of Slovenian Medical Association. - ISSN 1318-0347 (Letn. 71, št. 1, jan. 2002, str. 31-33)
    Vrsta gradiva - članek, sestavni del
    Leto - 2002
    Jezik - slovenski
    COBISS.SI-ID - 5383220

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