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    A Fatal Case of Generalized Lysosomal Storage Disease in an Infant. por Ponce Camacho, Marco Antonio, Melo de la Garza, Américo, Barboza Quintana, Álvaro, Barboza Quintana, Oralia, Ancer Rodríguez, Jesús, Ramírez Bon, Enrique, Garza Alatorre, Arturo Gerardo, Rodríguez Gutiérrez, Nora Alicia

    Publicado 2010
    “…Depending on the severity of the enzymatic defect, gangliosidoses show different rates of clinical progression and organ involvement; poor residual enzyme activity is seen in more aggressive forms (infantile and juvenile subtypes) leading to early death whereas cases with better residual enzyme activity have a late onset in adult life and a milder clinical course. …”
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