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Maxillofacial Dysostosis


content provided by Healthwise

Synonyms

  • Hypoplasia of the Maxilla, Primary Familial

Disorder Subdivisions

  • None

General Discussion

Maxillofacial Dysostosis is a rare disorder inherited as an autosomal dominant trait. Major characteristics include an underdeveloped upper jaw, delayed speech as well as poor articulation, down-slanting of the eyelids, and malformations of the external ear.



Resources

Children's Craniofacial Association

13140 Coit Road

Suite 517

Dallas, TX 75240

USA

Tel: (214)570-9099

Fax: (214)570-8811

Tel: (800)535-3643

Email: csmith@ccakids.com

Internet: http://www.ccakids.com



FACES: The National Craniofacial Association

P.O. Box 11082

Chattanooga, TN 37401

Tel: (423)266-1632

Fax: (423)267-3124

Tel: (800)332-2373

Email: faces@faces-cranio.org

Internet: http://www.faces-cranio.org



Forward Face, Inc.

317 East 34th Street

Room 901

New York, NY 10016

Tel: (212)684-5860

Fax: (212)684-5864

Tel: (800)393-3223

Email: info@forwardface.org

Internet: http://www.forwardface.org



Let's Face It (USA)

P.O. Box 29972

Bellingham, WA 98228-1972

USA

Tel: (360)676-7325

Email: faceit@umich.edu

Internet: http://www.dent.umich.edu/faceit



AmeriFace

PO Box 751112

Las Vegas, NV 89136

USA

Tel: (702)769-9264

Fax: (702)341-5351

Tel: (888)486-1209

Email: info@ameriface.org

Internet: http://www.ameriface.org



National Craniofacial Foundation

3100 Carlisle Street

Suite 215

Dallas, TX 75204

Tel: (800)535-3643



For a Complete Report

This is an abstract of a report from the National Organization for Rare Disorders, Inc. ® (NORD). 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 orphan@rarediseases.org

Last Updated:  2/14/2008

Copyright  1992, 2000 National Organization for Rare Disorders, Inc.


Last Updated: February 14, 2008


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