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Gaucher disease is the most common lysosomal storage disease. It was named for the French physician Phillipe Gaucher who first described it in 1882. The disease is caused by a lack of glucocerebrosidase, which causes a buildup of glucocerebroside in the tissues.

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Q: Who discovered the Gaucher's disease?
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How does a person receive the gauchers disease?

Gauchers disease is a genetic condition - it is not a 'communicable' disease, in that it can only be passed on through bloodlines.


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Gaucher disease is caused by a genetic defect in an enzyme called glucocerebroside. There are four different types of this disease. For more information about Gaucher disease visit Answers.com


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