Kód: 16549334
Gaucher disease (GD), the most common inherited lysosomal storage disorder, is a multiorgan disease due to an autosomal recessive defect of the gene encoding glucocerebrosidase enzyme. Our aim in this study is to spot light on the ... celý popis
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Gaucher disease (GD), the most common inherited lysosomal storage disorder, is a multiorgan disease due to an autosomal recessive defect of the gene encoding glucocerebrosidase enzyme. Our aim in this study is to spot light on the clinical and laboratory characteristics of children with Gaucher disease and to evaluate the outcome of enzyme replacement therapy in Iraq, As most of cases in the developing countries still under diagnosed.
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Osobní odběr Praha, Brno a 12903 dalších
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