腕部x线片显示手骨年龄;一个缺乏x射线的女孩

Hüsnü Maraşlı, N. Çelik, Yeşim Sidar Duman
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摘要

马德隆畸形(MD)是由于桡骨远端内侧和掌侧过早闭合所致它在女孩中更为常见和严重,通常在儿童中期/晚期发展MD是矮个子同形盒基因(SHOX)缺陷的最显著特征之一,它导致矮个子3。放射弓是一种著名的放射学未来。另一方面,SHOX缺乏的手部x线片有三种典型的放射学征象;月状骨的三角化、锥体化和远端桡骨的透光度。在对一名患有性早熟的9岁女孩的评估中,她的身高测量值为第18百分位。在确定患者骨龄的腕关节x线片上,其外观与MD相符(图1)。在MD患者的遗传学研究中,胰蛋白酶G带带技术显示正常女性核型(46,XX)。使用SHOX基因区域(Xp22.33)特异性探针,采用荧光原位杂交技术检测杂合子SHOX缺失。解释直接x线对识别MD很重要。因此,在矮小身材患者的病因学中更容易发现SHOX基因缺失。
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Wrist radiography for hand bone age tells a lot; a girl with SHOX deficiency
Madelung's deformity (MD) occurs as a result of premature closure of the medial and volar aspects of the distal radial physis.1 It is more frequent and severe in girls, and usually develops in middle/late childhood.2 MD is one of the most characteristic features of he short-stature homeobox gene (SHOX) deficiency, which causes short stature3. Radial bowing is one of the  well-known radiological futures. On the other hand, there are three typical radiological sign of the hand radiograph for SHOX deficiency; triangularization, pyramidalization of the os lunatum, and radiolucency at the distal radius4.      In the evaluation of a 9-year-old girl who was investigated for precocious puberty, her height measurement was 18th percentile. On the wrist X-ray taken for the determination of the bone age of the patient, there was an appearance compatible with MD (Figure 1). In the genetic studies of the patient with MD, normal female karyotyping (46, XX) was demonstrated by Trypsin G banding Technique. Heterozygous SHOX deletion was detected by Fluorescence In Situ Hybridization technique using a probe specific to the SHOX gene region (Xp22.33).      Interpreting the direct X-ray is important in recognizing the MD. Thus, it will be easier to detect SHOX gene deletion in the etiology of short stature patients with this deformity.
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