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Fig. 1 | BMC Neurology

Fig. 1

From: A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature review

Fig. 1

Clinical 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 spine

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BMC Neurology

ISSN: 1471-2377

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