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Gaucher disease

Glucocerebrosidase deficiency; Glucosylceramidase deficiency; Lysosomal storage disease - Gaucher

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Causes

Gaucher disease is rare in the general population. People of Eastern and Central European (Ashkenazi) Jewish heritage are more likely to have this disease.

It is an autosomal recessive disease. This means that the mother and father must both pass one abnormal copy of the disease gene to their child in order for the child to develop the disease. A parent who carries an abnormal copy of the gene but doesn't have the disease is called a silent carrier.

The lack of the glucocerebrosidase enzyme causes harmful substances to build up in the liver, spleen, bones, and bone marrow. These substances prevent cells and organs from working properly.

There are 3 main subtypes of Gaucher disease:

  • Type 1 is most common. It involves bone disease, anemia, an enlarged spleen and low platelets (thrombocytopenia). Type I affects both children and adults. It is most common in the Ashkenazi Jewish population.
  • Type 2 usually begins in infancy with severe neurologic involvement. This form can lead to rapid, early death.
  • Type 3 may cause liver, spleen, and brain problems. People with this type may live into adulthood.

Definition

Gaucher disease is a rare genetic disorder in which a person lacks an enzyme called glucocerebrosidase (GBA).

Exams and Tests

The health care provider will perform a physical exam and ask about the symptoms.

The following tests may be done: 

Outlook (Prognosis)

How well a person does depends on their subtype of the disease. The infantile form of Gaucher disease (Type 2) may lead to early death. Most affected children die before age 5.

Adults with the type 1 form of Gaucher disease can expect normal life expectancy with enzyme replacement therapy.

Possible Complications

Complications of Gaucher disease may include:

Prevention

Genetic counseling is recommended for prospective parents with a family history of Gaucher disease. Testing can determine if parents carry the gene that could pass on the Gaucher disease. A prenatal test can also tell if a baby in the womb has Gaucher syndrome.

Support Groups

For more information contact:

Symptoms

Bleeding because of low platelet count is the most common symptom seen in Gaucher disease. Other symptoms may include:

Treatment

Gaucher disease can't be cured. But treatments can help control and may improve symptoms.

Medicines may be given to:

  • Replace the missing GBA (enzyme replacement therapy) to help reduce spleen size, bone pain, and improve thrombocytopenia.
  • Limit production of fatty chemicals that build up in the body.

Other treatments include:

  • Medicines for pain
  • Surgery for bone and joint problems, or to remove the spleen
  • Blood transfusions 

Review Date: 10/30/2016
Reviewed By: Anna C. Edens Hurst, MD, MS, Assistant Professor in Medical Genetics, The University of Alabama at Birmingham, Birmingham, AL. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Isla Ogilvie, PhD, and the A.D.A.M. Editorial team.

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