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GD is a rare autosomal recessive disorder characterized by the defective function of the catabolic enzyme \u03b2-glucocerebrosidase (GBA), leading to an accumulation of its substrate, glucocerebroside. Clinical signs and symptoms include neurological dysfunctions, bone infarcts and malformations, hepatosplenomegaly and hypersplenism leading to anemia, neutropenia and thrombocytopenia. Enzyme replacement therapy with recombinant GBA is the mainstay of treatment for GD, which became the first successfully managed lipid storage disease. Future treatments may include oral enzyme replacement and\/or gene therapy interventions.<\/jats:p>","DOI":"10.1159\/000440865","type":"journal-article","created":{"date-parts":[[2015,11,20]],"date-time":"2015-11-20T22:01:25Z","timestamp":1448056885000},"page":"13-23","source":"Crossref","is-referenced-by-count":113,"title":["Gaucher Disease: Clinical, Biological and Therapeutic Aspects"],"prefix":"10.1159","volume":"83","author":[{"given":"Azza","family":"Dandana","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Souhaira","family":"Ben 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