It is possible that the main title of the report Campomelic 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.
- Campomelic Dwarfism
- Campomelic Dysplasia
- Campomelic Syndrome, Long-Limb Type
- Camptomelic Dwarfism
- Camptomelic Syndrome, Long-Limb Type
- Dwarfism, Campomelic
- Camptomelic Syndrome
- SRY-Box 9, SOX9 Mutations Syndrome
- Acampomelic campomelic "Dysplasia"
Campomelic syndrome is a rare congenital disorder in which multiple anomalies are present. It is characterized by bowing and angular shape of the long bones of the legs, especially the tibia; multiple minor anomalies of the face; cleft palate; other skeletal anomalies such as abnormalities of the shoulder and pelvic area and eleven pairs of ribs instead of the usual twelve; underdevelopment of the trachea; developmental delay in some cases and incomplete development of genitalia in males such that they appear to be females.
Human Growth Foundation
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Little People of America, Inc.
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NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases
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Coalition for Heritable Disorders of Connective Tissue (CHDCT)
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Washington, DC 20008
Genetic and Rare Diseases (GARD) Information Center
PO Box 8126
Gaithersburg, MD 20898-8126
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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
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Last Updated: 9/17/2007
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