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</div><div><span>Gaucher disease</span></div></div>
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<article><div id="d-article"><div class="page-info"><div class="page-title"><a name="start" id="start">
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</a><h1 class="with-also" itemprop="name">Gaucher disease</h1>
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</noscript></div><div class="main"><div id="ency_summary"><p>Gaucher disease is a rare genetic disorder in which a person lacks an enzyme called glucocerebrosidase (GBA).</p></div><section><div class="section"><div class="section-header"><div class="section-title"><h2>Causes</h2></div><div class="section-button"><button type="submit" aria-controls="section-1" role="button" title="Expand/Collapse section"><span class="icon icon-section-action">
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</div></div><div class="section-body" id="section-1"><p>Gaucher disease is rare in the general population. People of Eastern and Central European (Ashkenazi) Jewish heritage are more likely to have this disease.</p><p>It is an <a test="test" href="./002052.htm">autosomal recessive</a> 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.</p><p>The lack of the GBA causes harmful substances to build up in the liver, spleen, bones, and bone marrow. These substances prevent cells and organs from working properly.</p><p>There are three main subtypes of Gaucher disease:</p><ul><li>Type 1 is most common. It involves bone disease, anemia, an enlarged spleen and low platelets (thrombocytopenia). Type 1 affects both children and adults. It is most common in the Ashkenazi Jewish population.</li><li>Type 2 usually begins in infancy with severe neurologic involvement. This form can lead to rapid, early death.</li><li>Type 3 may cause liver, spleen, and brain problems. People with this type may live into adulthood. </li></ul></div></div></section><section><div class="section"><div class="section-header"><div class="section-title"><h2>Symptoms</h2></div><div class="section-button"><button type="submit" aria-controls="section-2" role="button" title="Expand/Collapse section"><span class="icon icon-section-action">
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</div></div><div class="section-body" id="section-2"><p>Bleeding because of low platelet count is the most common symptom seen in Gaucher disease. Other symptoms may include:</p><ul><li><a test="test" href="./003180.htm">Bone pain</a> and fractures</li><li>Cognitive impairment (decreased thinking ability)</li><li>Easy bruising</li><li><a test="test" href="./003276.htm">Enlarged spleen</a></li><li><a test="test" href="./003275.htm">Enlarged liver</a></li><li><a test="test" href="./003088.htm">Fatigue</a></li><li>Heart valve problems</li><li>Lung disease (rare)</li><li>Seizures</li><li>Severe <a test="test" href="./003103.htm">swelling</a> at birth</li><li>Skin changes</li></ul></div></div></section><section><div class="section"><div class="section-header"><div class="section-title"><h2>Exams and Tests</h2></div><div class="section-button"><button type="submit" aria-controls="section-3" role="button" title="Expand/Collapse section"><span class="icon icon-section-action">
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</div></div><div class="section-body" id="section-3"><p>The health care provider will perform a physical exam and ask about the symptoms.</p><p>The following tests may be done:</p><ul><li>Blood test to look for enzyme activity</li><li><a test="test" href="./003658.htm">Bone marrow aspiration</a></li><li><a test="test" href="./003335.htm">MRI</a></li><li><a test="test" href="./003330.htm">CT</a></li><li><a test="test" href="./003381.htm">X-ray of the skeleton</a></li><li>Genetic testing</li></ul></div></div></section><section><div class="section"><div class="section-header"><div class="section-title"><h2>Treatment</h2></div><div class="section-button"><button type="submit" aria-controls="section-4" role="button" title="Expand/Collapse section"><span class="icon icon-section-action">
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</div></div><div class="section-body" id="section-4"><p>Gaucher disease can't be cured. But treatments can help control and may improve symptoms.</p><p>Medicines may be given to:</p><ul><li>Replace the missing GBA (enzyme replacement therapy) to help reduce spleen size, bone pain, and improve thrombocytopenia.</li><li>Limit production of fatty chemicals that build up in the body.</li></ul><p>Other treatments include:</p><ul><li>Medicines for pain</li><li>Surgery for bone and joint problems, or to remove the spleen</li><li>Blood transfusions </li></ul></div></div></section><section><div class="section"><div class="section-header"><div class="section-title"><h2>Support Groups</h2></div><div class="section-button"><button type="submit" aria-controls="section-5" role="button" title="Expand/Collapse section"><span class="icon icon-section-action">
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</div></div><div class="section-body" id="section-5"><p>These groups can provide more information on Gaucher disease:</p><ul><li>National Gaucher Foundation -- <a class="extln" target="_blank" href="https://www.gaucherdisease.org">www.gaucherdisease.org</a></li><li>MedlinePlus - Gaucher disease.-- <a class="extln" target="_blank" href="https://medlineplus.gov/genetics/condition/gaucher-disease/">medlineplus.gov/genetics/condition/gaucher-disease/</a></li><li>National Organization for Rare Diseases -- rarediseases.org/rare-diseases/gaucher-disease <a class="extln" target="_blank" href="https://rarediseases.org/rare-diseases/gaucher-disease/?filter=ovr-ds-resources">rarediseases.org/rare-diseases/gaucher-disease</a></li></ul></div></div></section><section><div class="section"><div class="section-header"><div class="section-title"><h2>Outlook (Prognosis)</h2></div><div class="section-button"><button type="submit" aria-controls="section-6" role="button" title="Expand/Collapse section"><span class="icon icon-section-action">
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</div></div><div class="section-body" id="section-6"><p>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.</p><p>Adults with the type 1 form of Gaucher disease can expect normal life expectancy with enzyme replacement therapy.</p></div></div></section><section><div class="section"><div class="section-header"><div class="section-title"><h2>Possible Complications</h2></div><div class="section-button"><button type="submit" aria-controls="section-7" role="button" title="Expand/Collapse section"><span class="icon icon-section-action">
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</div></div><div class="section-body" id="section-7"><p>Complications of Gaucher disease may include:</p><ul><li><a test="test" href="./003200.htm">Seizures</a></li><li><a test="test" href="./000560.htm">Anemia</a></li><li><a test="test" href="./000586.htm">Thrombocytopenia</a></li><li>Bone problems</li></ul></div></div></section><section><div class="section"><div class="section-header"><div class="section-title"><h2>Prevention</h2></div><div class="section-button"><button type="submit" aria-controls="section-8" role="button" title="Expand/Collapse section"><span class="icon icon-section-action">
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</div></div><div class="section-body" id="section-8"><p><a test="test" href="../patientinstructions/000510.htm">Genetic counseling</a> 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.</p></div></div></section><section><div class="section"><div class="section-header"><div class="section-title"><h2>Alternative Names</h2></div><div class="section-button"><button type="submit" aria-controls="section-Alt" role="button" title="Expand/Collapse section"><span class="icon icon-section-action">
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</div></div><div class="section-body" id="section-Alt"><p>Glucocerebrosidase deficiency; Glucosylceramidase deficiency; Lysosomal storage disease - Gaucher; Gaucher's disease</p></div></div></section><section><div class="section sec-mb"><div class="section-header"><div class="section-title"><h2>Images</h2></div><div class="section-button"><button type="submit" aria-controls="section-tnails" role="button" title="Expand/Collapse section"><span class="icon icon-section-action">
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<li><img src="//medlineplus.gov/ency/images/ency/tnails/1450t.jpg" alt="Gaucher cell - photomicrograph" title="Gaucher cell - photomicrograph" class="side-img"/><a href="../imagepages/1450.htm">Gaucher cell - photomicrograph</a></li>
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<li><img src="//medlineplus.gov/ency/images/ency/tnails/1451t.jpg" alt="Gaucher cell - photomicrograph #2" title="Gaucher cell - photomicrograph #2" class="side-img"/><a href="../imagepages/1451.htm">Gaucher cell - photomicrograph #2</a></li>
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<li><img src="//medlineplus.gov/ency/images/ency/tnails/17215t.jpg" alt="Hepatosplenomegaly" title="Hepatosplenomegaly" class="side-img"/><a href="../imagepages/17215.htm">Hepatosplenomegaly</a></li>
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</ul></div></div></section><section><div class="section"><div class="section-header"><div class="section-title"><h2>References</h2></div><div class="section-button"><button type="submit" aria-controls="section-Ref" role="button" title="Expand/Collapse section"><span class="icon icon-section-action">
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</div></div><div class="section-body" id="section-Ref"><p>Kliegman RM, St. Geme JW, Blum NJ, Shah SS, Tasker RC, Wilson KM. Defects in metabolism of lipids. In: Kliegman RM, St. Geme JW, Blum NJ, Shah SS, Tasker RC, Wilson KM, eds. <em>Nelson Textbook of Pediatrics. </em>21st ed. Philadelphia, PA: Elsevier; 2020:chap 104.</p><p>Krasnewich DM, Sidransky E. Lysosomal storage diseases. In: Goldman L, Schafer AI, eds. <em>Goldman-Cecil Medicine. </em>26th ed. Philadelphia, PA: Elsevier; 2020:chap 197.</p><p>Turnpenny PD, Ellard S, Cleaver R. Inborn errors of metabolism. In: Turnpenny PD, Ellard S, Cleaver R, eds. <em>Emery's Elements of Medical Genetics and Genomics.</em> 16th ed. Philadelphia, PA: Elsevier; 2022:chap 18.</p></div></div></section>
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<section><div class="section"><div class="section-header"><div class="section-title"><h2>Review Date 10/13/2022</h2></div><div class="section-button"><button type="submit" aria-controls="section-version" role="button" title="Expand/Collapse section"><span class="icon icon-section-action">
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<div id="section-version" class="section-body"><p>Updated by: Anna C. Edens Hurst, MD, MS, Associate Professor in Medical Genetics, The University of Alabama at Birmingham, Birmingham, AL. Review provided by VeriMed Healthcare Network. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.</p>
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