It is possible that the main title of the report Achondrogenesis is not the name you expected.
Achondrogenesis is a group of rare disorders characterized by extreme short-limb dwarfism, abnormal development of ribs and other skeletal abnormalities. The health problems associated with these conditions are life-threatening and most affected infants die before birth, are stillborn or die shortly after birth of respiratory failure. Achondrogenesis type IA and type IB are autosomal recessive genetic conditions. Achondrogenesis type II is an autosomal dominant genetic condition.
Human Growth Foundation
997 Glen Cove Avenue
Glen Head, NY 11545
6645 W. North Avenue
Oak Park, IL 60302
Little People of America, Inc.
250 El Camino Real
Tustin, CA 92780
Restricted Growth Association
PO Box 1024
Peterborough, Intl PE1 9GX
Tel: 0300 111 1970
Fax: 0300 111 2454
Coalition for Heritable Disorders of Connective Tissue
4301 Connecticut Avenue, NW, Suite 404
Washington, DC 20008
Compassionate Friends - Supporting Family After A Child Dies
P.O. Box 3696
Oak Brook, IL 60522-3696
MUMS National Parent-to-Parent Network
150 Custer Court
Green Bay, WI 54301-1243
Genetic and Rare Diseases (GARD) Information Center
PO Box 8126
Gaithersburg, MD 20898-8126
PO Box 241956
Los Angeles, CA 90024
European Skeletal Dysplasia Network
Wellcome Trust Centre for Cell-Matrix Research
Faculty of Life Sciences
University of Manchester
Michael Smith Building, Oxford Road
Manchester, M13 9PT
Tel: 44 161 275 5642
Fax: 44 161 275 5082
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 email@example.com
Last Updated: 8/31/2010
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