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: 719
- Bone Diseases: 5863
  - Developmental Bone Diseases: 153
    - Osteochondrodysplasias: 592
      - Cleidocranial Dysplasia: 160
- Musculoskeletal Abnormalities: 43
  - Craniofacial Abnormalities: 203
    - Cleidocranial Dysplasia: 160
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Musculoskeletal Abnormalities: 43
    - Craniofacial Abnormalities: 203
      - Cleidocranial Dysplasia: 160

Carla Derech Selected Research

Carla Derech Research Topics

Disease

Therapy/Procedure