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Tayova-Sachsova choroba, AB variant

  1. Subject h.Tayova-Sachsova choroba, AB variant
    Subject h.Tay-Sachs Disease, AB Variant
    Entry termsTayova-Sachsova choroba, AB forma
    choroba z deficitu aktivátora proteínu GM2
    gangliozidóza GM2, AB variant
    gangliozidóza GM2, AB forma
    gangliozidóza GM2, typ AB
    gangliozidóza GM2 typu AB
    choroba z deficitu aktivátora proteínu GM2
    English X referencesGM2 Protein Activator Deficiency Disease
    Gangliosidosis GM2, AB Variant
    Gangliosidosis GM2, Type AB
    Scope note in EnglishA progressive neurodegenerative disorder that begins with muscle weakness, then progresses to startle reaction, retardation and seizures. It is characterized by the accumulation of G(M2) GANGLIOSIDE in neurons that is caused by a lack of G(M2) ACTIVATOR PROTEIN function. The AB variant designation refers to the increase of both HEXOSAMINIDASE A and HEXOSAMINIDASE B in tissues that lack of G(M2) activator protein.
    See also reference (FX) in Slovak proteín aktivátorový G(M2)
    See also reference (FX) in English G(M2) Activator Protein
    Links (1) - MeSH descriptor
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Number of the records: 1  

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