Cleidocranial dysplasia syndrome in 1 case.docVIP

 PAGE \* MERGEFORMAT 4 Cleidocranial dysplasia syndrome in 1 case Of: Science Shannon Tsai, Chung Kiu, Chen recorded Xing, Zhao Chunkui, WORLD ECONOMICS Liu Zhaoming, Fan Shifu [Keywords:] lock Lufa Yu insufficiency, deformity Cleidocranial dysplasia syndrome is a congenital malformation of bone, is a genetic disease in clinical practice is rare. I recently admitted to hospital and the other 1 case multiple bone Cleidocranial dysplasia cases, are as follows. A medical record Patients, male, 34 years old, married, because “the machine twisted with pain and hurt caused by dysfunction of the right forearm 2 h” admission. Admission generally in good condition, no special investigation cardiopulmonary abdomen, face smaller anterior fontanel is not closed, transverse thoracic diameter narrowing, bilateral nonunion of the clavicle were at home and abroad, and its medial thinning were to the right significantly, and push forward side of the double shoulder mobility increases, the left lower limb shortening of about 3 cm, right forearm swelling, see false joint activities. Patients family of grandparents, parents, brothers and no similar history, the son of the face in patients with small, eyebrow distance increases, not to further track the history. auxiliary examination: X-ray film prompted the right radius and ulna fractures; further action related to X-ray film Check the tips below. (1 head: craniosynostosis widened anterior fontanel is not closed, shown in Figure 1, (2 clavicle: Bilateral clavicle and the acromion client does not even have the right medial clavicle were fine, Figure 2, ( 3 Pelvis: pelvic dysplasia of the bone, pubic symphysis distance increases, about 1.5 cm, sacroiliac joint space increased approximately 0.6 cm; the left acetabulum lighter, smaller left femoral head, greater trochanter and femoral shaft, etc. Up side shift, shown in Figure 3, (4 spine: C5 ~ 7 and T1 vertebral body such as spina bifida, shown in Figure 4. line the ri