
Cleidocranial dysplasia (CCD) is a rare autosomal dominant dysplasia with an estimated incidence of 1:1,000,000. Prominent features include large head with delayed suture closure, persistent metopic suture, Wormian bones, hypertelorism, small face, cleft mandible, dental dysplasia, hypoplasia or aplasia of the clavicles, hypoplastic scapula with a small glenoid, cleft sternum, coxa vara or valga, a narrow pelvis, delayed pubic ossification, and several varieties of spinal abnormalities. We report a case of a 30-year-old male patient with this syndrome.
Medicine (General), Wormian Bones, R5-920, Autosomal Dominant, Cleidocranial Dysplasia, Internal medicine, RC31-1245
Medicine (General), Wormian Bones, R5-920, Autosomal Dominant, Cleidocranial Dysplasia, Internal medicine, RC31-1245
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