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Pierre Robin sequence with severe scoliosis in an adult: A case report of clinical and radiological features

机译:成年人严重脊柱侧弯的Pierre Robin序列:临床和放射学特征的病例报告

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摘要

Pierre Robin sequence (PRS) is characterized by the triad of micrognathia, glossoptosis, and airway obstruction. PRS does not have a single pathogenesis, but rather is associated with multiple syndromes. This report presents the case of a 35-year-old woman with PRS and scoliosis. Among the syndromes related to PRS, cerebro-costo-mandibular syndrome (CCMS), which is characterized by posterior rib gap defects and vertebral anomalies, was suspected in this patient. However, no posterior rib gap defect was detected on radiological examinations. Although over 80 cases of CCMS have been reported to date, few cases of PRS with scoliosis alone have been reported. Therefore, this report demonstrated the clinical, radiological, and cephalometric characteristics of an adult patient with PRS and scoliosis, but without rib anomalies.
机译:皮埃尔·罗宾(Pierre Robin)序列(PRS)的特征是微念珠菌性黑质,视光吞噬和气道阻塞。 PRS没有单一的发病机制,而是与多种综合征相关。该报告介绍了一名35岁的女性,患有PRS和脊柱侧弯。在与PRS相关的综合征中,怀疑该患者患有脑肋下颌综合征(CCMS),其特征是后肋间隙缺损和椎骨异常。但是,放射学检查未发现后肋间隙缺损。尽管迄今为止已报告了80多例CCMS病例,但仅报道了很少有脊柱侧弯的PRS病例。因此,本报告证明了患有PRS和脊柱侧弯但无肋骨异常的成年患者的临床,影像学和头颅测量特征。

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