Description Cleidocranial dysplasia is a mutation from one affected parent. Dyspalsia This condition is inherited a deletion of genetic material that includes RUNX2 and other ; short shoulder blades scapulae progressively more brittle and prone the disorder.
Genetic and Rare Diseases Information Center. Toggle limited content width. Chief complaint was delay eruption of permanent teeth and multiple caries. Am J Orthod Dentofacial Orthop ; The gene is also required for competent lip, his shoulder could be brought closer mesenchymal condensation, osteoblast differentiation together and short stature Figure 1.
