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Pediatric Sleep Surgery: Skeletal Procedures

机译:小儿睡眠手术:骨骼程序

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摘要

Skeletal abnormalities are rare but often correctable causes of pediatric obstructive sleep apnea (OSA). Any facial abnormality that leads to airway impingement may contribute to OSA. The most common congenital craniofacial diagnoses associated with OSA are Robin sequence and syndromic craniosynostosis (SCS). Robin sequence (RS) is defined as the triad of micrognathia (small and retropositioned mandible), glossoptosis (tongue positioned superiorly and posteriorly such that it occludes the oropharynx), and airway obstruction. The incidence of RS ranges from 1:8500 to 1:14,000 live births. Although not a defining characteristic of RS, a cleft of the secondary palate is present in more than 90% of affected individuals.
机译:骨骼异常是罕见的,但通常是儿科阻塞性睡眠呼吸暂停(OSA)的可矫正原因。 任何导致气道调节的面部异常都可能有助于OSA。 与OSA相关的最常见的先天性颅面诊断是Robin序列和综合征颅骨肌肤源(SCS)。 Robin序列(RS)定义为MicroMathathia(小和亲新的下颌骨)的三联,华丽促(舌头上方和后部定位,使其遮挡oropharynx)和气道阻塞。 卢比的发病率为1:8500至1:14,000个活产出生。 虽然不是Rs的定义特征,但在超过90%的受影响的个体中存在裂隙的裂隙。

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