Suppr超能文献

锁骨颅骨发育不全患儿颅骨的发育情况

Development of the skull in infants with cleidocranial dysplasia.

作者信息

Jensen B L, Kreiborg S

机构信息

Department of Pediatric Dentistry, School of Dentistry, University of Copenhagen, Denmark.

出版信息

J Craniofac Genet Dev Biol. 1993 Apr-Jun;13(2):89-97.

PMID:8325972
Abstract

The purpose of the present paper is to clarify some of the questions regarding pathogenesis in cleidocranial dysplasia (CCD) in order to improve the understanding of the mechanisms leading to the craniofacial abnormalities characteristic for young and adult patients with the syndrome. The neonatal skull is described and craniofacial development from birth to 7 years analyzed. Skull radiographs of 11 CCD patients ages 0-7 years were examined. Study methods included plain radiographs of the skull and roentgencephalometric films in the lateral, frontal, and axial projections. In one patient, CT scans of the skull with 3-D reconstructions were available. Common to the four patients examined within the first 6 months postnatally was a marked delay of skeletal maturity. In the calvaria a severe reduction of calcification in all bones was found. Corresponding to the expected sutural areas, gaping defects were recorded, indicating that calcification of calvarial bones in the newborn CCD individual had only reached a stage corresponding to around 20 weeks gestational age. Calvarial size corresponded to that of normal newborns and the morphology was relatively normal, taking into account the pronounced deformation that took place during parturition due to the soft, undermineralized skull. At birth bony islands could be observed in the periphery of the occipital, parietal, and frontal bones. Ossification of the maxilla and the mandible seemed to be within normal limits. Posteriorly to the foramen magnum, the chondral part of the supraoccipital bone remained unossified. In the cranial base an increased width of the spheno-occipital synchondrosis was found.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本文的目的是阐明一些关于锁骨颅骨发育不全(CCD)发病机制的问题,以增进对导致该综合征的年轻和成年患者颅面异常机制的理解。描述了新生儿颅骨,并分析了从出生到7岁的颅面发育情况。检查了11例年龄在0至7岁的CCD患者的颅骨X光片。研究方法包括颅骨的平片以及侧位、正位和轴位的X线头影测量片。有一名患者可获得颅骨的CT扫描及三维重建图像。出生后6个月内检查的4例患者的共同特点是骨骼成熟明显延迟。在颅盖骨中,发现所有骨骼的钙化严重减少。在预期的缝合区域,记录到明显的间隙缺损,这表明新生儿CCD个体的颅盖骨钙化仅达到相当于孕龄约20周的阶段。考虑到由于颅骨柔软、矿化不足在分娩过程中发生明显变形,颅盖骨大小与正常新生儿相当,形态相对正常。出生时,可在枕骨、顶骨和额骨周边观察到骨岛。上颌骨和下颌骨的骨化似乎在正常范围内。枕骨大孔后方,枕骨上部的软骨部分仍未骨化。在颅底,发现蝶枕软骨结合增宽。(摘要截选至250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验