Gaucher’s Disease Type 3

Gauchers-Disease-Type-3

Gaucher’s disease is a rare, inherited disorder in which you do not have enough of an enzyme called glucocerebrosidase. This causes too much of a fatty substance to build up in your spleen, liver, lungs, bones and, sometimes, your brain.

Gaucher’s disease is a rare, inherited disorder in which you do not have enough of an enzyme called glucocerebrosidase. This causes too much of a fatty substance to build up in your spleen, liver, lungs, bones and, sometimes, your brain. This prevents these organs from working properly.

There are three types:

Type 1, the most common form, causes liver and spleen enlargement, bone pain and broken bones, and, sometimes, lung and kidney problems. It does not affect the brain. It can occur at any age.
Type 2, which causes severe brain damage, appears in infants. Most children who have it die by age 2.
In type 3, there may be liver and spleen enlargement. The brain is gradually affected. It usually starts in childhood or adolescence. Gaucher’s disease has no cure. Treatment options for types 1 and 3 include medicine and enzyme replacement therapy, which is usually very effective. There is no good treatment for the brain damage of types 2 and 3.

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2 thoughts on “Gaucher’s Disease Type 3

  1. Perneet says:

    Hi i am looking for medicine or treatment details for Gaucher disease Type 1

    • Select the disease/s you suffer from: Gaucher\'s Disease Type 1
    • Which language do you prefer to get the answer?: English
    • Premilife Customer Care says:

      Dear Perneet
      Thank you for approaching us.
      We have answered your question in a personal mail sent to you.
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      If you have further questions, please feel free contacting us using the Contact Premilife page. We will be happy to assist.
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