Cleidocranial dysostosis
A rare autosomal dominant disorder caused by mutations in the RUNX2 gene. It is characterized by developmental abnormalities in the bones and teeth, including the complete or partial absence of the clavicles, delayed closure of the fontanels, protruding mandible, hypertelorism, scoliosis, and short stature.
Disease Alternative Name
Recent Cases of Cleidocranial dysostosis
Browse recently discussed Cleidocranial dysostosis cases by specialists16 Views
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B.SC;BDS;PGDMLC;Cerficate Implantology
Govt Dental College Osmania
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Self Employed. Now Doing My Practice
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MKCG MCH
MBBS and MD (pediatrics)
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Deihori Model Hospital
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