Cri du Chat Syndrome
National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Cri du Chat Syndrome is not the name you expected.
Cri du chat syndrome (CdCS or 5p-) is a rare genetic disorder in which a variable portion of the short arm of chromosome 5 is missing or deleted (monosomic). Symptoms vary greatly from case to case depending upon the exact size and location of the deleted genetic material. Common symptoms include a distinctive cry that resembles the mewing of a cat, characteristic facial features, slow growth, and microcephaly, a condition that indicates that head circumference is smaller than would be expected for an infant's age and sex. Affected children also exhibit delays in the acquisition of skills requiring the coordination of muscular and mental activities (psychomotor disability) and moderate to severe intellectual disability. Additional symptoms affecting different organ systems of the body can also occur. Most cases are thought arise from spontaneous (de novo) genetic errors very early in embryonic development.
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- Lakewood, CA 90714
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- Fax: (562)920-5240
- Tel: (888)970-0777
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- Website: http://www.fivepminus.org
Chromosome Disorder Outreach, Inc.
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Cleft Lip and Palate Foundation of Smiles
- 2044 Michael Ave SW
- Wyoming, MI 49509
- Tel: (616)329-1335
- Email: Rachelmancuso09@comcast.net
- Website: http://www.cleftsmile.org
Cri Du Chat Syndrome Support Group
- PO Box 3408
- Norwich, NR3 3WE
- United Kingdom
- Tel: 8450942725
- Fax: 1455841680
- Email: firstname.lastname@example.org
- Website: http://www.criduchat.org.uk/
Department of Human Genetics/Cri du Chat
- Medical College of Virginia
- P.O. Box 980033
- Richmond, VA 23298
- Tel: (804)828-8116
- Fax: (804)828-8801
Genetic and Rare Diseases (GARD) Information Center
- PO Box 8126
- Gaithersburg, MD 20898-8126
- Tel: (301)251-4925
- Fax: (301)251-4911
- Tel: (888)205-2311
- Website: http://rarediseases.info.nih.gov/GARD/
March of Dimes
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- Website: http://www.thearc.org
UNIQUE - Rare Chromosome Disorder Support Group
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- United Kingdom
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For a Complete Report
This is an abstract of a report from the National Organization for Rare Disorders (NORD). For a full-text version of this report, go to www.rarediseases.org and click on Rare Disease Database under "Rare Disease Information".
The information provided in this report is not intended for diagnostic purposes. It is provided for informational purposes only.
It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report.
This disease entry is based upon medical information available through the date at the end of the topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database completely current and accurate. Please check with the agencies listed in the Resources section for the most current information about this disorder.
Last Updated: 6/14/2011
Copyright 2011 National Organization for Rare Disorders, Inc.
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