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Gaucher disease type I
- 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 ...
- Gaucher disease is an inherited disorder that affects many of the body's organs and tissues. The signs and symptoms of this condition vary widely among affected ...
- 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 ...
- 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)Gaucher Disease/Learn More ... Gaucher Disease ... Health Problems in Pregnancy/Related Issues ... Health Problems in Pregnancy ... Organization of Teratology Information ...
- 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 ...
(National Human Genome Research Institute) 