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Gaucher disease type III
- Gaucher Disease (National Library of Medicine)Gaucher disease is a rare, inherited disorder. It is a type of lipid metabolism disorder. If you have ... affected. It usually starts in childhood or adolescence. Gaucher disease has no cure. Treatment options for types 1 ...
- ... I; GD1 GAUCHER DISEASE, TYPE II; GD2 GAUCHER DISEASE, TYPE III; GD3 GAUCHER DISEASE, TYPE IIIC; GD3C PubMed Beutler E. Gaucher ...
- Gaucher disease is a rare genetic disorder in which a person lacks an enzyme called glucocerebrosidase (GBA). ... Gaucher disease is rare in the general population. People of Eastern and Central European (Ashkenazi) Jewish heritage are ...
- Learning about Gaucher Disease (National Human Genome Research Institute)Gaucher Disease/Learn More ... Gaucher Disease ... National Human Genome Research Institute ... From the National Institutes of Health ... Gaucher disease is an autosomal ...
- Lipid Metabolism Disorders (National Library of Medicine)... with this process. Lipid metabolism disorders, such as Gaucher disease and Tay-Sachs disease, involve lipids. Lipids are ...
- Gaucher Disease and Pregnancy (Organization of Teratology Information Specialists)Health Problems in Pregnancy/Related Issues ... Health Problems in Pregnancy ... Gaucher Disease/Learn More ... Gaucher Disease ... Organization of Teratology Information ...
- ClinicalTrials.gov: Gaucher Disease (National Institutes of Health)Gaucher Disease/Clinical Trials ... Gaucher Disease
- ... a disorder that resembles a severe form of Gaucher disease. Signs and symptoms of this condition include neurological ... as it does in the classic form of Gaucher disease. A few PSAP gene mutations have also been ...
- Miglustat is used to treat Gaucher disease type 1 (a condition in which a certain fatty substance is not broken down normally in the body and instead builds ...
- Eliglustat is used to treat Gaucher disease type 1 (a condition in which a certain fatty substance is not broken down normally in the body and builds up ...