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epilepsie myoklonické progresívne

  1. Subject h.epilepsie myoklonické progresívne
    Subject h.Myoclonic Epilepsies, Progressive
    Entry termsMayov-Whiteov syndróm
    myoklonus akčný spojený so zlyhaním obličiek
    myoklónia akčná spojená so zlyhaním obličiek
    encefalopatia reagujúca na biotín
    encefalopatia responzívna na biotín
    atrofia dentátorubrálna-palidoluyziánska
    English X referencesAction Myoclonus-Renal Failure Syndrome
    Biotin-Responsive Encephalopathy
    Dentatorubral-Pallidoluysian Atrophy
    May-White Syndrome
    Scope note in EnglishA heterogeneous group of primarily familial EPILEPSY disorders characterized by myoclonic seizures, tonic-clonic seizures, ataxia, progressive intellectual deterioration, and neuronal degeneration. These include LAFORA DISEASE; MERRF SYNDROME; NEURONAL CEROID-LIPOFUSCINOSIS; sialidosis (see MUCOLIPIDOSES), and UNVERRICHT-LUNDBORG SYNDROME.
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