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特纳综合征患儿颅面复合体的形态

Shape of the craniofacial complex in children with Turner syndrome.

作者信息

Rongen-Westerlaken C, vd Born E, Prahl-Andersen B, Rikken B, Teunenbroek V, Kamminga N, vd Tweel I, Otten B J, Delamarre vd Waal H A, Drayer N M

机构信息

Department of Paediatrics, University Hospital Nijmegen, The Netherlands.

出版信息

J Biol Buccale. 1992 Dec;20(4):185-90.

PMID:1306180
Abstract

The shape of the craniofacial complex was established in 69 children with Turner syndrome aged between 3.5 and 16.6 years. The children had not been treated with growth hormone (GH) or anabolic steroids. On a standardized lateral roentgenencephalogram 13 linear and 7 angular variables were measured. Data of all variables were available from normal Dutch children for comparison. The main abnormalities were located in the cranial base and in the mandible and consisted of a short posterior cranial base, all increased cranial base angle and a short, retrognathic and posteriorly rotated mandible. The maxilla was smaller than normal and also slightly posteriorly rotated. The abnormalities were already present in young children with Turner syndrome. Indications were found that in Turner syndrome interstitially as well as appositionally growing cartilage is affected. The changes in the maxilla can be explained in various ways. They may be due to defective growth of the nasal cartilage or to a disorder in the intramembranous ossification of the maxilla or they may be adaptive to the changes in the cranial base and the mandible. From this study it can be concluded that patients with Turner syndrome exhibit several craniofacial abnormalities, probably due to a cartilage disorder.

摘要

对69名年龄在3.5至16.6岁之间的特纳综合征患儿的颅面复合体形态进行了研究。这些患儿未接受过生长激素(GH)或合成代谢类固醇治疗。在标准化的头颅侧位X线片上测量了13个线性变量和7个角度变量。所有变量的数据均可从正常荷兰儿童中获取以作比较。主要异常位于颅底和下颌骨,包括后颅底短、颅底角均增大、下颌骨短、后缩且向后旋转。上颌骨比正常小且也略向后旋转。这些异常在特纳综合征幼儿中就已存在。有迹象表明,在特纳综合征中,间质性生长和表面生长的软骨均受到影响。上颌骨的变化可以用多种方式来解释。它们可能是由于鼻软骨生长缺陷,或者是上颌骨膜内成骨紊乱,或者可能是对上颌骨和下颌骨变化的适应性改变。从这项研究可以得出结论,特纳综合征患者表现出几种颅面异常,可能是由于软骨疾病所致。

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