Fig. 1From: A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature reviewClinical pictures and radiologic findings for the index patient with CCD. a The photographs show a flat face, sunken nasal bridge, hypertelorism, chin protrusion, and sloping shoulders. Arrows indicate atrophy of bilateral shoulder girdle muscles. b Chest X-ray shows the absent right clavicle (arrow) and a hypoplastic left clavicle. c Skull X-ray shows wormian bones in the skull (left panel) and a hypoplastic maxilla (right panel). d Spine X-ray reveals mild scoliosis of the thoraco-lumbar spineBack to article page