Articles liés à Gaucher Disease in Iraqi Children

Gaucher Disease in Iraqi Children - Couverture souple

Farhan, Rabab; Jamal, Ausama

 
9783330043398: Gaucher Disease in Iraqi Children

Synopsis

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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Présentation de l'éditeur

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.

Biographie de l'auteur

Assistant Prof. Dr. Rabab Farhan graduated from collage of medicine/ Baghdad university 1983, Candidate of Arab board in Pediatrics 1993.Assistant Professor of Pediatric Gastroenterology and liver disease/ Medical collage/ University of Baghdad. Consultant Pediatric gastroenterology in Children Welfare Teaching Hospital, Medical city, Baghdad.

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