Campomelic Dysplasia

A congenital disorder of CHONDROGENESIS and OSTEOGENESIS characterized by hypoplasia of endochondral bones. In most cases there is a curvature of the long bones especially the TIBIA with dimpling of the skin over the bowed areas, malformation of the pelvis and spine, 11 pairs of ribs, hypoplastic scapulae, club feet, micrognathia, CLEFT PALATE, tracheobronchomalacia, and in some patients male-to-female sex reversal (SEX REVERSAL, GONADAL). Most patients die in the neonatal period of respiratory distress. Campomelic dysplasia is associated with haploinsufficiency of the SOX9 TRANSCRIPTION FACTOR gene.

Also Known As:

Acampomelic Campomelic Dysplasia; Campomelic Dwarfism; Campomelic Syndrome; Camptomelic Dysplasia; Cmpd1 Sra1; Acampomelic Campomelic Dysplasias; Campomelic Dwarfisms; Campomelic Dysplasia, Acampomelic; Campomelic Dysplasias; Campomelic Dysplasias, Acampomelic; Campomelic Syndromes; Camptomelic Dysplasias; Cmpd1 Sra1s; Dwarfism, Campomelic; Dwarfisms, Campomelic; Dysplasia, Acampomelic Campomelic; Dysplasia, Campomelic; Dysplasia, Camptomelic; Dysplasias, Acampomelic Campomelic; Dysplasias, Campomelic; Dysplasias, Camptomelic; Sra1, Cmpd1; Sra1s, Cmpd1; Syndrome, Campomelic; Syndromes, Campomelic

Musculoskeletal Diseases: 719
- Musculoskeletal Abnormalities: 43
  - Campomelic Dysplasia: 43
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Musculoskeletal Abnormalities: 43
    - Campomelic Dysplasia: 43

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Drug/Important Bio-Agent (IBA)