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Cleidocranial dysplasia (CCD) is a rare autosomal dominant inherited disorder, characterized primarily by general retardation in bone ossification, hypoplastic clavicles and various craniofacial and dental abnormalities. Even though most cases are diagnosed during childhood or adolescence, newborn infants may present with symptoms of respiratory distress due to chest deformity, needing intensive care unit treatment.






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Cleidocranial dysplasia (CCD) causing respiratory distress syndrome in a newborn infant. A case report.

Free full text article: Cleidocranial dysplasia (CCD) causing respiratory distress syndrome in a newborn infant. A case report.

Abstract
Cleidocranial dysplasia (CCD), also known as Scheuthauer Marie-Sainton Syndrome, is a rare autosomal dominant inherited disorder, characterized by general retardation in bone ossification, hypoplastic clavicles and various craniofacial and dental abnormalities. Early diagnosis of CCD can be difficult, because the majority of craniofacial abnormalities become obvious only during adolescence. We present a rare case of CCD with neonatal manifestation and would like to promote the awareness of this rare disorder and the importance of early diagnosis.






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