Definition: 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.
Other names Dysostosis, Cleidocranial; Cleidocranial Dysostosis; Syndrome, Scheuthauer-Marie-Sainton; Syndrome, Marie-Sainton; Scheuthauer Marie Sainton Syndrome; Marie Sainton Syndrome; Dysplasias, Cleidocranial; Dysplasia, Cleidocranial; Dysostosis, Cleidocranial Digital; Dysostoses, Cleidocranial Digital; Dysostoses, Cleidocranial; Cleidocranial Dysplasias; Cleidocranial Dysostoses; Cleidocranial Digital Dysostoses; Scheuthauer-Marie-Sainton Syndrome; Marie-Sainton Syndrome; Cleidocranial Digital Dysostosis
