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Gauchers disease - Wikipedia Gaucher's disease or Gaucher disease ( ɡoʊˈʃeɪ ) (GD) is a genetic disorder in which glucocerebroside (a sphingolipid, also known as glucosylceramide) accumulates in cells and certain organs
Gaucher Disease: Symptoms, Causes Treatment - Cleveland Clinic Gaucher disease (pronounced “go-shay”) is an inherited lysosomal storage disorder (LSD), a type of disease that causes fatty substances (sphingolipids) to build up in your bone marrow, liver and spleen The sphingolipids weaken bones and enlarge your organs, so they can’t work as they should
Gaucher Disease - Johns Hopkins Medicine Gaucher disease is a rare genetic disorder passed down from parents to children (inherited) When you have Gaucher disease, you are missing an enzyme that breaks down fatty substances called lipids Lipids start to build up in certain organs such as your spleen and liver
National Gaucher Foundation Gaucher disease is a genetic disorder and affects the body's organs and tissues Learn about Gaucher disease symptoms, testing and treatments
What is Gaucher disease? | Gaucher Disease News Gaucher disease is caused by mutations in the GBA1 gene, which lead to the accumulation of certain fatty molecules that drive organ damage and disease symptoms Gaucher disease is a rare disorder The global Gaucher disease prevalence is estimated to be about 1 5 out of every 100,000 live births
Gaucher disease: MedlinePlus Genetics 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 individuals
Gaucher Basics - Childrens Gaucher Research Fund Gaucher (pronounced “go-shay”) Disease is a genetic disorder, which results in the deficiency in an enzyme, causing a portion of old cells to be stored in areas such as the liver, spleen, lungs, lymph system, and bones instead of being expelled from the body
Gaucher disease type I | About the Disease | GARD Gaucher disease is caused by changes in the GBA gene and is inherited in an autosomal recessive manner Diagnosis is suspected by clinical symptoms and confirmed by measuring GBA enzyme activity or genetic testing