Jensen B L, Kreiborg S
Department of Pediatric Dentistry, School of Dentistry, University of Copenhagen, Denmark.
J Craniofac Genet Dev Biol. 1993 Apr-Jun;13(2):98-108.
The purpose of the present investigation is to describe and discuss the craniofacial abnormalities in young and adult patients with cleidocranial dysplasia (CCD). Skull radiographs of 52 CCD patients were examined. Thirty-six patients were adult, 16 were between 7 and 16 years old. Facial photographs were available in 30 cases, and in one adult case with cranial CT scans, 3-D reconstructions were carried out. High quality photographs of six CCD skulls were also described. The paranasal sinuses were absent or diminished in all children and most adult patients. An inverted pear-shape of the calvaria and an open anterior fontanelle were present in more than 60% of the cases. In the cranial base an upward distortion of the clivus, an anteverted foramen magnum, and extremely narrow choanae were frequent traits, together with small sella and bulbous dorsum sellae. Nearly all patients and dry skulls showed hypoplasia or absence of nasal bones. The zygomatic arches were diminished or incomplete in all cases. Mandibular morphology was judged to be syndrome specific with the slender, upward-backward-pointing coronoid process. We have concluded that a great part of the abnormal qualitative traits are present to a lesser degree in CCD children, indicating a progressive abnormal development with advancing age. From the present and previous studies on CCD we have hypothesized that on top of their generalized reduction of growth potential, these patients suffer from a combination of skeletal immaturity resulting in deformations and a defective bone remodeling. We have acknowledged the importance of longitudinal investigations in order to ameliorate the understanding of the pathogenesis of CCD and thereby to improve total patient care. Correction of the craniofacial abnormalities may be advocated in the most severe cases of hypertelorism and midfrontal groove, if psychosocial problems occur. Also, patients with major midface underdevelopment might benefit from combined orthodontic/surgical correction.
本研究的目的是描述和讨论患有锁骨颅骨发育不全(CCD)的青少年和成年患者的颅面异常情况。对52例CCD患者的颅骨X光片进行了检查。36例为成年人,16例年龄在7至16岁之间。30例有面部照片,1例成年患者有头颅CT扫描,并进行了三维重建。还描述了6个CCD颅骨的高质量照片。所有儿童和大多数成年患者的鼻窦缺如或发育不全。超过60%的病例存在颅骨呈倒梨形和前囟未闭。在颅底,斜坡向上扭曲、枕骨大孔前倾和后鼻孔极窄是常见特征,同时蝶鞍小且鞍背呈球茎状。几乎所有患者和干燥颅骨均显示鼻骨发育不全或缺如。所有病例的颧弓均变窄或不完整。下颌形态被认为具有综合征特异性,其冠突细长且向上向后指向。我们得出结论,很大一部分异常定性特征在CCD儿童中程度较轻,表明随着年龄增长存在渐进性异常发育。根据目前及以往对CCD的研究,我们推测除了生长潜力普遍降低外,这些患者还存在骨骼发育不成熟导致的变形和骨重塑缺陷的综合问题。我们认识到纵向研究对于增进对CCD发病机制的理解从而改善患者整体护理的重要性。在最严重的两眼间距过宽和额中部沟的病例中,如果出现心理社会问题,可主张矫正颅面异常。此外,主要中面部发育不全的患者可能会从正畸/手术联合矫正中受益。