软骨发育不全患者颅面形态的形态学分析。

M M Cohen, G F Walker, C Phillips
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引用次数: 0

摘要

人软骨发育不全可以看作是研究软骨内异常成骨对颅骨整体发育影响的实验模型。在本研究中,将25名成年男性和26名成年女性软骨发育不全患者的侧位脑电图转换为颅面形态的二维坐标模型,并使用66个线性、角度和面积变量进行分析。采用951例正常成人侧位脑电图进行比较。采用两个样本t检验比较软骨发育不全的脑电图与正常脑电图。多元统计分析包括Hotelling’s T2和判别函数分析。选择的变量被绘制为剖面模式,其中平均值表示为相对于规范的标准偏差单位(Z分数)。最后,使用Calcomp图进行视觉检查,并将男性和女性软骨发育不全受试者与正常男性和女性受试者的平均头测图进行比较。软骨发育不全的重要表现包括颅骨增大、额部隆起、额窦大、枕突、前颅底长度正常、后颅底长度明显缩短、颅底角尖锐、鼻骨短且变形凹陷、上面部高度短、上颌骨凹陷、鼻底后倾斜、前突下颌骨向前移位,但大小正常,角正常,冠突高。在软骨发育不全的受试者中发现正常的前颅底长度是令人惊讶的,因为颅底是在软骨中形成的,发育不全和缩短是意料之中的。由于软骨发育不全患者的大脑增大,额叶的扩大可能影响前颅底的生长,因为它遵循神经生长模式。筛状板的长度显著减少,但蝶骨前部的长度显著增加,这弥补了筛状板长度的缩短,表明颅底前部长度的增长主要是通过一个部位的适应而发生的,即蝶筛软骨联合症。后颅底长度明显短被解释为由于软骨中预先形成的骨发育不全,可能导致蝶骨-枕关节联合早期关闭。软骨发育不全患者颅底角的过度闭合可能与脑体积增大有关,并且可能比正常的蝶间软骨联合更早闭合。(摘要删节为400字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A morphometric analysis of the craniofacial configuration in achondroplasia.

Human achondroplasia can be viewed as an experimental model for studying the effects of abnormal endochondral bone formation on the development of the skull as a whole. In this study, lateral cephalograms of 25 adult males and 26 adult females with achondroplasia were converted to a two-dimensional coordinate model of craniofacial morphology and analyzed using 66 linear, angular, and area variables. Lateral cephalograms of 951 normal adults were used for comparison. Two sample t-tests were used to compare achondroplastic cephalograms with normal cephalograms. Multivariate statistical analysis included Hotelling's T2 and discriminant function analysis. Selected variables were graphed as profile patterns in which mean values were expressed as standard deviation units (Z scores) relative to the norm. Finally, Calcomp plots were used for visual inspection and for comparison of the average cephalometric tracings of male and female achondroplastic subjects with normal male and female subjects, respectively. Significant findings in achondroplasia included enlarged calvaria, frontal bossing, large frontal sinuses, occipital prominence, normal anterior cranial base length, strikingly shortened posterior cranial base length, an acute cranial base angle, a short nasal bone that was deformed and depressed, short upper facial height, recessed maxilla, posterior tilt of the nasal floor, and a prognathic mandible that was anteriorly displaced but of normal size with a normal gonial angle and a high coronoid process. The finding of normal anterior cranial base length in achondroplastic subjects was surprising since the cranial base is preformed in cartilage and hypoplasia and shortening would be expected. Since the brain is enlarged in achondroplasia, the expanding frontal lobes may possibly influence the growth of the anterior cranial base, since it is known to follow a neural pattern of growth. Cribriform plate length was strikingly reduced, but anterior sphenoidal length was strikingly increased, compensating for the shortened cribriform plate length and suggesting that growth in the length of the anterior cranial base takes place primarily by adaptation at one site--namely, the sphenoethmoidal synchondrosis. Strikingly short posterior cranial base length was interpreted as resulting from hypoplasia of bone that is preformed in cartilage with possible early closure of the spheno-occipital synchondrosis. The exaggerated closure of the cranial base angle in achondroplasia may be related to an increased brain size and possibly earlier than normal closure of the intersphenoidal synchondrosis.(ABSTRACT TRUNCATED AT 400 WORDS)

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