Cleidocranial Dysplasia

Autosomal dominant syndrome in which there is delayed closing of the CRANIAL FONTANELLES; complete or partial absence of the collarbones (CLAVICLES); wide PUBIC SYMPHYSIS; short middle phalanges of the fifth fingers; and dental and vertebral anomalies.

Also Known As:

Cleidocranial Dysostosis; Cleidocranial Digital Dysostosis; Marie-Sainton Syndrome; Scheuthauer-Marie-Sainton Syndrome; Cleidocranial Digital Dysostoses; Cleidocranial Dysostoses; Cleidocranial Dysplasias; Dysostoses, Cleidocranial; Dysostoses, Cleidocranial Digital; Dysostosis, Cleidocranial Digital; Dysplasia, Cleidocranial; Dysplasias, Cleidocranial; Marie Sainton Syndrome; Scheuthauer Marie Sainton Syndrome; Syndrome, Marie-Sainton; Syndrome, Scheuthauer-Marie-Sainton; Dysostosis, Cleidocranial

Musculoskeletal Diseases: 751
- Bone Diseases: 5970
  - Developmental Bone Diseases: 156
    - Osteochondrodysplasias: 604
      - Cleidocranial Dysplasia: 164
- Musculoskeletal Abnormalities: 46
  - Craniofacial Abnormalities: 208
    - Cleidocranial Dysplasia: 164
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Congenital Abnormalities: 26404
  - Musculoskeletal Abnormalities: 46
    - Craniofacial Abnormalities: 208
      - Cleidocranial Dysplasia: 164

N Bilahari Selected Research

N Bilahari Research Topics

Disease

Therapy/Procedure