In this video, we delve into Gaucher Disease, a lysosomal storage disorder caused by a deficiency of the enzyme glucocerebrosidase. This deficiency leads to the accumulation of glucocerebroside in various organs, particularly the spleen, liver, and bone marrow.

Discover the common symptoms, such as anemia, fatigue, and bone pain, as well as the different types of Gaucher Disease (Type 1, Type 2, and Type 3) and the latest treatment options, including enzyme replacement therapy and substrate reduction therapy.

Whether you're a patient, caregiver, or simply curious, our goal is to provide you with clear and comprehensive information.

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