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Otopalatodigital Syndrome Type I and II
National Organization for Rare Disorders, Inc.
- Cranioorodigital Syndrome
- Faciopalatoosseous Syndrome
- OPD Syndrome
- OPD Syndrome, Type I
- OPD Syndrome, Type II
Otopalatodigital syndrome type I and II are rare X-linked genetic disorders in which complete expression of the disease occurs only in males. Females may be mildly affected with some of the symptoms. OPD type I is the milder form of the disease and is characterized by cleft palate, hearing loss and skeletal abnormalities in the skull and limbs. OPD type II includes these abnormalities as well as growth deficiency and abnormalities of the brain and is frequently not compatible with life.
Children's Craniofacial Association
13140 Coit Road
Dallas, TX 75240
FACES: The National Craniofacial Association
PO Box 11082
Chattanooga, TN 37401
Let's Face It
School of Dentistry / Dentistry Library
1011 N. University
Concord, MA 01742
National Foundation for Facial Reconstruction
333 East 30th Street, Lobby Unit
New York, NY 10016
Oto Palatal Digital Syndrome Family Resource Network
9559 Woodridge Circle
Eden Prairie, MN 55347
Genetic and Rare Diseases (GARD) Information Center
PO Box 8126
Gaithersburg, MD 20898-8126
Let Them Hear Foundation
1900 University Avenue, Suite 101
East Palo Alto, CA 94303
American Academy of Audiology
11730 Plaza America Drive, Suite 300
Reston, VA 20190
For a Complete Report
This is an abstract of a report from the National Organization for Rare Disorders, Inc.® (NORD). Cigna members can access the complete report by logging into myCigna.com. For non-Cigna members, a copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html.
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: 5/21/2008
Copyright 1992, 2004 National Organization for Rare Disorders, Inc.