首页> 外文期刊>Pediatric radiology >Radiographic findings and Gs-alpha bioactivity studies and mutation screening in acrodysostosis indicate a different etiology from pseudohypoparathyroidism.
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Radiographic findings and Gs-alpha bioactivity studies and mutation screening in acrodysostosis indicate a different etiology from pseudohypoparathyroidism.

机译:放射影像学发现,Gs-alpha生物活性研究和肩突固定症的突变筛查表明其病因与假性甲状旁腺功能减退症不同。

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摘要

Acrodysostosis is an uncommon skeletal dysplasia associated with nasal hypoplasia, midface deficiency, severe brachydactyly, and varying degrees of hearing loss and mental retardation. Previous publications have suggested that it may be difficult to distinguish acrodystostosis from pseudohypoparathyroidism on clinical grounds, but acrodysostosis does appear to have distinct clinical and radiologic findings. Spinal stenosis is an underappreciated risk in acrodysostosis, despite the reported loss of normal caudal widening of the lumbar interpediculate distance on AP spine radiographs in the original report of this disorder by Robinow et al., with confirmation of these radiographic findings by Butler et al. We report two sporadic cases of acrodysostosis, one of which required decompressive laminectomy for symptomatic spinal stenosis, and review 11 cases of acrodysostosis from 9 families that were submitted to the International Skeletal Dysplasia Registry. The objective of this report is to determine the frequency and severity of spinal stenosis in patients with acrodysostosis and to summarize the clinical and radiographic findings of acrodysostosis in an effort to distinguish acrodysostosis clearly from pseudohypoparathyroidism. The pattern of brachydactyly differs between these two conditions, and varying degrees of spinal stenosis are characteristic of acrodysostosis. Both our index patients with acrodysostosis had normal bioactivity of the alpha subunit of the Gs protein, therefore indicating that acrodysostosis has a different pathogenesis from pseudohypoparathyroidism. Furthermore, single-strand confirmational polymorphism (SSCP) analysis failed to demonstrate any confirmational alterations in the coding exons of the Gs alpha gene. These radiographic and laboratory findings substantiate that acrodysostosis is clinically different from pseudohypoparathyroidism and that it is necessary to follow patients with acrodysostosis for signs of spinal stenosis.
机译:肢端不全症是一种罕见的骨骼发育不良,与鼻发育不全,中面部缺乏,严重的近距离性肢体发育以及不同程度的听力下降和智力低下有关。先前的出版物表明,从临床上可能很难将肩dy骨固定症与假性甲状旁腺功能减退区分开,但是肩dy骨固定症的确在临床和影像学上有明显的发现。尽管Robinow等人在该疾病的原始报告中报告了AP脊柱X光片上正常的尾椎加宽,但腰椎椎弓根距离的正常尾部变宽丧失,但脊柱狭窄是肩峰狭窄风险的低估,Butler等人证实了这些影像学发现。我们报告了2例散发性肢端不全症,其中1例需要对症状性椎管狭窄进行减压椎板切除术,并回顾了9个家庭的11例肢端不全症,这些病例已提交至国际骨骼发育不良注册处。本报告的目的是确定肩峰狭窄患者的椎管狭窄的频率和严重程度,并总结肩峰发育不良的临床和影像学表现,以期将肩峰狭窄与假性甲状旁腺功能减退症区分开来。在这两种情况下,近距离触诊的模式不同,并且不同程度的椎管狭窄是肢端固定的特征。我们的两名患有肩突固定症的患者均具有正常的Gs蛋白α亚基生物活性,因此表明肩突固定症的发病机制与假性甲状旁腺功能减退症不同。此外,单链确证多态性(SSCP)分析未能证明Gs alpha基因编码外显子的任何确证变化。这些影像学检查和实验室检查结果证实,肩峰固定症在临床上与假性甲状旁腺功能减退症不同,并且有必要追踪肩峰固定症患者以发现椎管狭窄的迹象。

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