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If the above diagnoses are inconclusive or if a treatment regimen has already been started, a biopsy of the affected skin (i.e. Spray tub and bathroom floor with disinfectant after each use to help prevent reinfection and infection of other household members.
Wash feet, particularly between the toes, with soap and dry thoroughly after bathing or showering. If you have experienced an infection previously, you may want to treat your feet and shoes with over-the-counter drugs. Dry feet well after showering, paying particular attention to the web space between the toes. Try to limit the amount that your feet sweat by wearing open-toed shoes or well-ventilated shoes, such as lightweight mesh running shoes. After any physical activity shower with a soap that has both an antibacterial and anti-fungal agent in it.


Type 1 Gaucher disease is the most common form of the disorder, and occurs more frequently in people of Ashkenazi (eastern and central European) Jewish heritage than in those with other backgrounds. Type 1 Gaucher Disease is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. Many women aren't diagnosed with Type 1 Gaucher disease until they are pregnant when hematologic issues, like anemia and low platelet count, become more apparent.
Type 1 Gaucher's Disease is the most common, accounting for 90 percent of all cases, and generally the mildest, with almost no effects on the brain.
Gaucher disease is very effectively treated with infusions of enzyme replacement therapy (ERT). Type 1 Gaucher disease is the most common form of this condition; it's also called non-neuronopathic Gaucher disease. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition.Mutations in the GBA gene cause Gaucher disease.


Prolonged treatment, over the course of two to four years, has been shown to reduce the rate of bone loss, improve bone pain and reduce bone crises. About 1 in 1,000 in Ashkenazi Jews are affected by this disease, and about 1 in 12 Ashkenazi Jews are carriers. Patients may also be treated with an oral medication called substrate reduction therapy that removes the accumulated fatty substance from the body.
It's encouraged that prospective parents meet with a genetic counselor and get tested before conception. This condition ranges from mild to severe and may appear anytime from childhood to adulthood.



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