Cohen M M, Walker G F, Phillips C
J Craniofac Genet Dev Biol Suppl. 1985;1:139-65.
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)
人类软骨发育不全可被视为一个实验模型,用于研究软骨内骨形成异常对整个颅骨发育的影响。在本研究中,对25名成年男性和26名成年女性软骨发育不全患者的头颅侧位片进行转换,构建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。选取951名正常成年人的头颅侧位片作为对照。采用两样本t检验比较软骨发育不全患者与正常对照的头颅侧位片。多变量统计分析包括霍特林T2检验和判别函数分析。将选定变量绘制成轮廓图,其中平均值以相对于正常的标准差单位(Z值)表示。最后,使用Calcomp绘图进行视觉检查,并分别比较男性和女性软骨发育不全患者与正常男性和女性受试者的平均头影测量描记图。软骨发育不全的显著表现包括颅骨增大、额部隆起、额窦增大、枕部突出、前颅底长度正常、后颅底长度显著缩短、颅底角变锐、鼻骨短且变形凹陷、面中高度短、上颌后缩、鼻底后倾以及下颌前突但大小正常、下颌角正常且冠突高。软骨发育不全患者前颅底长度正常这一发现令人惊讶,因为颅底由软骨预先形成,预计会发育不全和缩短。由于软骨发育不全患者大脑增大,额叶扩展可能会影响前颅底的生长,因为已知前颅底遵循神经生长模式。筛板长度显著缩短,但蝶骨前部长度显著增加,补偿了缩短的筛板长度,提示前颅底长度的增长主要通过一个部位——即蝶筛软骨结合处的适应性变化来实现。后颅底长度显著缩短被解释为软骨预先形成的骨发育不全,可能伴有蝶枕软骨结合处过早闭合。软骨发育不全中颅底角过度闭合可能与大脑尺寸增加有关,也可能与蝶间软骨结合处比正常更早闭合有关。(摘要截选至400字)