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Gaucher Disease

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NORD is very grateful to Dr. Roscoe Brady from the NIH office of NINDS for assistance in updating this report.

Synonyms of Gaucher Disease
  • Cerebroside Lipidosis Syndrome
  • Gaucher splenomegaly
  • Glucocerebrosidase deficiency
  • Glucocerebrosidosis
  • Glucosylceramidase deficiency
  • Glucosyl cerebroside lipidosis
  • Kerasin lipoidosis
  • Kerasin thesaurismosis
  • Lipid histiocytosis (kerasin type)
  • Sphingolipidosis 1

Disorder Subdivisions

  • Norrbottnian Gaucher Disease
  • Type I Gaucher Disease
  • Type II Gaucher Disease
  • Type III Gaucher Disease


General Discussion
Gaucher disease is a rare, inherited metabolic disorder in which deficiency of the enzyme glucocerebrosidase results in the accumulation of harmful quantities of certain fats (lipids), specifically the glycolipid glucocerebroside, throughout the body especially within the bone marrow, spleen and liver. The symptoms and physical findings associated with Gaucher disease vary greatly from case to case. Some individuals will develop few or no symptoms (asymptomatic); others may have serious complications. Common symptoms associated with Gaucher disease include an abnormally enlarged liver and/or spleen (hepatosplenomegaly), low levels of circulating red blood cells (anemia), low levels of platelets(thrombocytopenia), and skeletal abnormalities. Platelets are blood cells that promote clotting and patients with thrombocytopenia may develop bleeding problems. Three separate forms of Gaucher disease have been identified and are distinguished by the absence of, or the presence and extent of, neurological complications. All three forms of Gaucher disease are inherited as autosomal recessive traits.

Gaucher disease is categorized as a lysosomal storage disorder. Lysosomes are the major digestive units in cells. Enzymes within lysosomes break down or "digest" nutrients, including certain complex carbohydrates and fats. In Gaucher disease certain fats, known as glycolipids, abnormally accumulate in the body because of the lack of the enzyme, glucocerebrosidase. This accumulation or "storage" of lipids leads to the various symptoms or physical findings associated with a lysosomal storage disease. Gaucher disease is the most common type of lysosomal storage disorder.
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Organizations related to Gaucher Disease
  • Arc (a national organization on mental retardation)
    1010 Wayne Ave
    Suite 650
    Silver Spring MD 20910
    Phone #: 301-565-3842
    800 #: 800-433-5255
    e-mail: info@thearc.org
    Home page: http://www.thearc.org/
  • Cochrane Cystic Fibrosis and Genetic Disorders Group
    Institute of Child Health, University of Liverpool
    Alder Hey Children's NHS Foundation Trust
    Liverpool None L12 2 AP
    Phone #: +44- (0-) 151 252 5696
    800 #: --
    e-mail: nikkij@liverpool.ac.uk
    Home page: http://www.cfgd.cochrane.org/en/index.html
  • Gauchers Association (UK)
    3 Bull Pitch
    Dursley
    Gloucestershire Intl GL11 4NG
    Phone #: 44 -145-3 549231
    800 #: --
    e-mail: ga@gaucher.org.uk
    Home page: http://www.gaucher.org.uk
  • Genetic and Rare Diseases (GARD) Information Center
    PO Box 8126
    Gaithersburg MD 20898-8126
    Phone #: 301-251-4925
    800 #: 888-205-2311
    e-mail: ordr@od.nih.gov
    Home page: http://rarediseases.info.nih.gov/Default.aspx
  • Hide & Seek Foundation for Lysosomal Disease Research
    6475 East Pacific Coast Highway Suite 466
    Long Beach CA 90803
    Phone #: 877-621-1122
    800 #: N/A
    e-mail: info@hideandseek.org
    Home page: http://www.hideandseek.org
  • Instituto de Errores Innatos del Metabolismo
    Carrera 7 No 40 - 62
    Bogota None None
    Phone #: (57-1) -3208320
    800 #: N/A
    e-mail: abarrera@javeriana.edu.co
    Home page: http://www.javeriana.edu.co
  • MUMS (Mothers United for Moral Support, Inc) National Parent-to-Parent Network
    150 Custer Court
    Green Bay WI 54301-1243
    Phone #: 920-336-5333
    800 #: 877-336-5333
    e-mail: mums@netnet.net
    Home page: http://www.netnet.net/mums/
  • Madisons Foundation
    PO Box 241956
    Los Angeles CA 90024
    Phone #: 310-264-0826
    800 #: N/A
    e-mail: getinfo@madisonsfoundation.org
    Home page: http://www.madisonsfoundation.org
  • March of Dimes Birth Defects Foundation
    1275 Mamaroneck Avenue
    White Plains NY 10605
    Phone #: 914-997-4488
    800 #: 888-663-4637
    e-mail: Askus@marchofdimes.com
    Home page: http://www.marchofdimes.com
  • National Gaucher Foundation
    2227 Idlewood Road
    Suite 12
    Tucker GA 30084
    Phone #: 770-934-2910
    800 #: 800-504-3189
    e-mail: ngf@gaucherdisease.org
    Home page: http://www.gaucherdisease.org
  • National Institute of Neurological Disorders and Stroke (NINDS)
    P.O. Box 5801
    Bethesda MD 20824
    Phone #: 301-496-5751
    800 #: 800-352-9424
    e-mail: me20t@nih.gov
    Home page: http://www.ninds.nih.gov/
  • National Tay-Sachs and Allied Diseases Association, Inc.
    2001 Beacon Street
    Suite 204
    Brighton MA 02135
    Phone #: 617-277-4463
    800 #: 800-906-8723
    e-mail: info@ntsad.org
    Home page: http://www.NTSAD.org
  • Sjældne Diagnoser / Rare Disorders Denmark
    Frederiksholms Kanal 2, 3rd Floor
    Copenhagen K None 1220
    Phone #: 45 -33 -14 00 10
    800 #: N/A
    e-mail: mail@sjaeldnediagnoser
    Home page: http://www.raredisorders.dk
  • Vaincre Les Maladies Lysosomales
    2 ter avenue de Fance
    Massy None 91300
    Phone #: 01 -69 -75 40 30
    800 #: --
    e-mail: accueil@vml-asso.org
    Home page: http://www.vml-asso.org

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Last modified Wednesday, November 26, 2008