8:50Gaucher disease is an inherited, rare, and serious disorder in humans that causes severe and debilitating symptoms, including enlargement of the liver and spleen, bone disease, easy bruising, and anemia.1 Individuals affected with this rare disease may not even know it exists and can suffer for years without a clear diagnosis.
Although people from every race and ethnic group are affected by Gaucher disease, it occurs more frequently in people of Ashkenazi (Eastern and Central European) Jewish descent than those of other backgrounds. In the Ashkenazi Jewish population, Type 1 Gaucher disease affects 1 in 600 people. Also, approximately 1 in 15 Ashkenazi Jews is a carrier.2,3
As families come together during this holiday season, improving awareness for Gaucher disease and its signs and symptoms, among the most affected populations, can help more patients achieve a faster diagnosis so they can begin their path to treatment.
Dr. Can Ficicioglu will discuss:
Gaucher disease and how it is inheritedThe signs and symptoms of the disease that families should be aware ofDiagnosis and treatment that families should keep in mind