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[脊椎胸廓发育不良——两例患病姐妹20年随访病例报告]

[Spondylothoracic dysplasia--a case report of 2 affected sisters with 20 year follow-up].

作者信息

Götze C, Götze H G

机构信息

Klinik und Poliklinik für Allgemeine Orthopädie der, I Westfälischen Wilhelms-Universität Münster.

出版信息

Z Orthop Ihre Grenzgeb. 2001 May-Jun;139(3):248-51. doi: 10.1055/s-2001-16329.

Abstract

This is a case report and review of the literature in spondylothoracic dysplasia. Spondylothoracic dysplasia is a genetically transmitted, rare entity characterized by multiple vertebral abnormalities and rib anomalies. Two siblings from one family of normal parents who have four other normal children were affected. There is no history of congenital anomalies in the family. Due to progressing deformity of the spine, a convex epiphyseodesis had to be performed in the oldest girl. The second girl, who has a healthy twin sister, was borne with an inperforated anus and a recto-vaginal fistula. An operation was performed at an early stage. Today, the mature patients are painfree and fully integrated in social life. Spondylothoracic dysplasia is discussed with regard to the hereditary nature, course, and prognosis on the basis of the pertinent literature.

摘要

这是一篇关于脊椎胸廓发育不良的病例报告及文献综述。脊椎胸廓发育不良是一种遗传性罕见疾病,其特征为多个椎体异常和肋骨畸形。来自一个父母正常且另有四个正常孩子的家庭中的两名兄弟姐妹患病。该家族无先天性异常病史。由于脊柱畸形进展,不得不对年龄较大的女孩进行凸侧骨骺阻滞术。第二个女孩与其健康的双胞胎姐姐出生时患有肛门闭锁和直肠阴道瘘,早期进行了手术。如今,成年患者无痛且完全融入社会生活。本文基于相关文献对脊椎胸廓发育不良的遗传性质、病程及预后进行了讨论。

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