Jaschke W
Z Kinderchir. 1985 Feb;40(1):60-2. doi: 10.1055/s-2008-1059715.
The genesis and clinical characteristics of Scheuthauer-Marie-Sainton's syndrome (dysostosis cleido-cranialis), of congenital pseudoarthrosis of the clavicula of post-traumatic clavicular pseudoarthrosis in childhood determine the differential diagnostic considerations of pseudoarthrosis in children in cases which are initially not clear. The therapy is, however, independent of the cause of the disease: Resection of the pseudoarthrotic bone, filling of the defect via a cortico-spongious block and stabilisation via plate osteosynthesis.
舒特豪尔-玛丽-桑顿综合征(锁骨颅骨发育不全)、先天性锁骨假关节或儿童创伤后锁骨假关节的发病机制及临床特征,决定了对儿童期起初不明原因的假关节进行鉴别诊断时需考虑的因素。然而,治疗与疾病病因无关:切除假关节骨,通过皮质松质骨块填充缺损,并通过钢板接骨术进行固定。