X-linked Opitz G/BBB syndrome
National Organization for Rare Disorders, Inc.
It is possible that the main title of the report X-linked Opitz G/BBB syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
Synonyms Back to top
- Opitz BBBG syndrome
- Opitz-G syndrome
- telecanthus-hypospadius syndrome (obsolete)
- hypertelorism-hypospadius syndrome (obsolete)
Disorder Subdivisions Back to top
General Discussion Back to top
X-linked Opitz G/BBB syndrome is a rare genetic disorder characterized by facial anomalies, respiratory and genitourinary abnormalities and other midline defects as well as developmental delay or mental retardation. There is a wide variation in severity of this condition, even among members of the same family. X-linked Opitz G/BBB syndrome is an X-linked genetic condition associated with alterations (mutations) in the MID1 gene.
Resources Back to top
Children's Craniofacial Association
13140 Coit Road
Dallas, TX 75240
FACES: The National Craniofacial Association
PO Box 11082
Chattanooga, TN 37401
1660 L Street, NW, Suite 301
Washington, DC 20036
Post Office Box 751112
Limekiln, PA 19535
Cleft Palate Foundation
1504 East Franklin Street
Chapel Hill, NC 27514-2820
National Foundation for Facial Reconstruction
333 East 30th Street, Lobby Unit
New York, NY 10016
123 Edward Street, Suite 1003
Ontario, M5G 1E2
Tel: (416) 597-2229
Fax: (416) 597-8494
Tel: (800) 665-3223
Genetic and Rare Diseases (GARD) Information Center
PO Box 8126
Gaithersburg, MD 20898-8126
Cleft Lip and Palate Foundation of Smiles
2044 Michael Ave SW
Wyoming, MI 49509
For a Complete Report Back to top
This is an abstract of a report from the National Organization for Rare Disorders (NORD). A copy of the complete report can be downloaded free from the NORD website for registered users. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational therapies (if available), and references from medical literature. For a full-text version of this topic, 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. NORD recommends that affected individuals seek the advice or counsel of their own personal physicians.
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.
For additional information and assistance about rare disorders, please contact the National Organization for Rare Disorders at P.O. Box 1968, Danbury, CT 06813-1968; phone (203) 744-0100; web site www.rarediseases.org or email email@example.com
Last Updated: 11/17/2012
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