Gaucher disease (GD) is a rare, genetic lysosomal disorder leading to lipid accumulation and dysfunction in multiple organs. Involvement of the skeleton is one of the most prevalent aspects of GD and a major cause of pain, disability, and reduced quality of life. Uniform recommendations for contemporary evaluation and management are needed. To develop practical clinical recommendations, an international group of experienced physicians conducted a comprehensive review of 20 years’ of the literature, defining terms according to pathophysiological understanding and pointing out best practice and unmet needs related to the skeletal features of this disorder. Abnormalities of bone modeling, reduced bone density, bone infarction, and plasma cell ...
Gaucher disease type 1 (GD1) is a rare inherited disease caused by mutations in the GBA1 gene, which...
Gaucher’s disease is a rare inherited lysosomal storage disease due to a genetic deficiency of...
Gaucher disease (GD) is caused by pathogenic mutations in GBA1, the gene that encodes the lysosomal ...
Gaucher disease (GD) is a rare, genetic lysosomal disorder leading to lipid accumulation and dysfunc...
Gaucher disease (GD) is a rare, genetic lysosomal disorder leading to lipid accumulation and dysfunc...
Gaucher disease is a rare autosomal recessive disorder of glycosphingolipid metabolism resulting fro...
Aim:Gaucher disease (GD) is the most prevalent hereditary lysosomal storage disorder, affecting mult...
Gaucher disease is a rare autosomal recessive disorder of glycosphingolipid metabolism resulting fro...
Gaucher disease is a rare autosomal recessive disorder of glycosphingolipid metabolism resulting fro...
Gaucher disease is a relatively rare metabolic disease caused by the inherited deficiency of the lys...
Gaucher disease is a relatively rare metabolic disease caused by the inherited deficiency of the lys...
Gaucher disease (GD) is an autosomal recessively inherited lysosomal disorder caused by mutations in...
Gaucher disease (GD) is the most prevalent lysosomal storage disease, and bone involvement is the mo...
Gaucher disease (GD) is caused by mutations in the gene GBA1, which encodes for the synthesis of the...
Gaucher, the most prevalent lysosomal disorder, is an autosomal recessive inherited disorder due to ...
Gaucher disease type 1 (GD1) is a rare inherited disease caused by mutations in the GBA1 gene, which...
Gaucher’s disease is a rare inherited lysosomal storage disease due to a genetic deficiency of...
Gaucher disease (GD) is caused by pathogenic mutations in GBA1, the gene that encodes the lysosomal ...
Gaucher disease (GD) is a rare, genetic lysosomal disorder leading to lipid accumulation and dysfunc...
Gaucher disease (GD) is a rare, genetic lysosomal disorder leading to lipid accumulation and dysfunc...
Gaucher disease is a rare autosomal recessive disorder of glycosphingolipid metabolism resulting fro...
Aim:Gaucher disease (GD) is the most prevalent hereditary lysosomal storage disorder, affecting mult...
Gaucher disease is a rare autosomal recessive disorder of glycosphingolipid metabolism resulting fro...
Gaucher disease is a rare autosomal recessive disorder of glycosphingolipid metabolism resulting fro...
Gaucher disease is a relatively rare metabolic disease caused by the inherited deficiency of the lys...
Gaucher disease is a relatively rare metabolic disease caused by the inherited deficiency of the lys...
Gaucher disease (GD) is an autosomal recessively inherited lysosomal disorder caused by mutations in...
Gaucher disease (GD) is the most prevalent lysosomal storage disease, and bone involvement is the mo...
Gaucher disease (GD) is caused by mutations in the gene GBA1, which encodes for the synthesis of the...
Gaucher, the most prevalent lysosomal disorder, is an autosomal recessive inherited disorder due to ...
Gaucher disease type 1 (GD1) is a rare inherited disease caused by mutations in the GBA1 gene, which...
Gaucher’s disease is a rare inherited lysosomal storage disease due to a genetic deficiency of...
Gaucher disease (GD) is caused by pathogenic mutations in GBA1, the gene that encodes the lysosomal ...