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Homocystinuria due to Cystathionine Beta-Synthase Deficiency

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NORD is very grateful to Jan P. Kraus, PhD, Professor of Pediatrics, University of Colorado, for assistance in the preparation of this report.

Synonyms of Homocystinuria due to Cystathionine Beta-Synthase Deficiency
  • Classical Homocystinuria
  • cystathionine beta-synthase deficiency
  • homocystinuria

Disorder Subdivisions



General Discussion
Homocystinuria is a rare metabolic condition characterized by an excess of the compound homocystine in the urine. The condition may result from deficiency of any of several enzymes involved in the conversion of the essential amino acid methionine to another amino acid (cysteine)--or, less commonly, impaired conversion of the compound homocysteine to methionine. Enzymes are proteins that accelerate the rate of chemical reactions in the body. Certain amino acids, which are the chemical building blocks of proteins, are essential for proper growth and development.

In most cases, homocystinuria is caused by reduced activity of an enzyme known as cystathionine beta-synthase (CBS). Infants who develop homocystinuria due to CBS deficiency (which is also known as classical homocystinuria) may fail to grow and gain weight at the expected rate (failure to thrive) and have developmental delays. By approximately age three, additional, more specific symptoms and findings may become apparent. These may include partial dislocation (subluxation) of the lens of the eyes (ectopia lentis), associated “quivering” (iridodonesis) of the colored region of the eyes (iris), severe nearsightedness (myopia), and other eye (ocular) abnormalities. Although intelligence may be normal in some cases, many children may be affected by progressive mental retardation. In addition, some may develop psychiatric disturbances and/or episodes of uncontrolled electrical activity in the brain (seizures). Affected individuals also tend to be thin with unusually tall stature; long, slender fingers and toes (arachnodactyly); and elongated arms and legs (“marfanoid” features). In addition, affected individuals may be at risk for the development of blood clots that can become lodged within certain large and small blood vessels (thromboembolisms), potentially leading to life-threatening complications. Homocystinuria due to deficiency of CBS deficiency is inherited as an autosomal recessive trait. The disorder is caused by changes (mutations) of a gene on the long arm (q) of chromosome 21 (21q22.3) that regulates the production of the CBS enzyme.

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Organizations related to Homocystinuria due to Cystathionine Beta-Synthase Deficiency
  • Arc
    1660 L Street, NW, Suite 301
    Washington DC 20036
    Phone #: 202-534-3700
    800 #: 800-433-5255
    e-mail: info@thearc.org
    Home page: http://www.thearc.org
  • Belgian Association for Metabolic Diseases (BOKS)
    Alice Nahonlann 7
    Melsele None 9120
    Phone #: 323-775-4839
    800 #: N/A
    e-mail: info@boks.be
    Home page: http://www.boks.be
  • CLIMB (Children Living with Inherited Metabolic Diseases)
    Climb Building
    176 Nantwich Road
    Crewe Intl CW2 6BG
    Phone #: 084-5 2-41 2174
    800 #: 080-0 6-52 3181
    e-mail: info.svcs@climb.org.uk
    Home page: http://www.CLIMB.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: http://rarediseases.info.nih.gov/GARD/EmailForm.aspx
    Home page: http://rarediseases.info.nih.gov/GARD
  • 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 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/
  • Save Babies Through Screening Foundation
    P.O. Box 42197
    Cincinnati OH 45242
    Phone #: 610-251-9876
    800 #: 888-454-3383
    e-mail: emails@savebabies.org
    Home page: http://www.savebabies.org

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Last modified Wednesday, November 26, 2008