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首页> 外文期刊>Clinical dysmorphology >Expanding the phenotype of spondylospinal thoracic dysostosis (the Turkel-Chen-Johnson syndrome)
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Expanding the phenotype of spondylospinal thoracic dysostosis (the Turkel-Chen-Johnson syndrome)

机译:扩大脊柱椎体胸椎发育不全的表型(Turkel-Chen-Johnson综合征)

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摘要

Spondylospinal thoracic dysostosis can be considered a type of spondylocostal dysostosis because of the occurrence of vertebral defects (hemivertebrae and vertebral body fusion) and thoracic anomalies (short thorax and pulmonary hypoplasia). This syndrome was described by Johnson et al. (1997) in two siblings with dwarfism, short thorax, curved spine, fusion of the vertebrae and spinal process, multiple pterygium, and arthrogryposis. We describe the case of a 16-year-old Mexican girl with the longest survival recorded (the previous oldest patient was 7 years old) and analyze the natural history and describe some new features of this rare entity. (C) 2014 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
机译:由于椎体缺损(半椎骨和椎体融合)和胸腔异常(胸廓短和肺发育不全)的发生,脊椎脊髓胸椎发育不全可被认为是脊椎肋骨软骨发育不全的一种。 Johnson等人描述了这种综合征。 (1997年)在两个兄弟姐妹与侏儒症,短胸,弯曲的脊柱,椎和脊柱融合,多发性翼状,肉和关节炎。我们描述了一个16岁的墨西哥女孩,其记录的生存时间最长(先前最大的患者是7岁),并分析了自然史并描述了这个罕见实体的一些新特征。 (C)2014 Wolters Kluwer Health垂直条Lippincott Williams&Wilkins。

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