Posnick J C, Ruiz R L
Posnick Center for Facial Plastic Surgery, Chevy Chase, Maryland 20815, USA.
Cleft Palate Craniofac J. 2000 Sep;37(5):433. doi: 10.1597/1545-1569(2000)037<0433:TCDSCS>2.0.CO;2.
Craniofacial dysostosis is the term applied to familial forms of craniosynostosis in which the sutural involvement generally includes the cranial vault, cranial base, and midfacial skeletal structures. The syndromic forms of craniofacial dysostosis were initially described by Carpenter, Apert, Crouzon, Saethre and Chotzen, Pfeiffer, and others. In addition to the dysmorphic cranial features, affected individuals may have profound alterations in facial skeletal development. Surgical reconstruction requires thoughtfully sequenced and staged procedures with consideration for the individual's specific malformations, craniofacial growth patterns, and psychosocial needs. Management of the craniofacial dysostosis syndromes is surgical, but the indications and the timing, type, and effectiveness of each stage of reconstruction have not been well evaluated and remains as much an art as a science. This article reviews the specific characteristic clinical features of the craniofacial dysostosis syndromes and presents current philosophy and rationale for the staging of reconstruction.
颅面骨发育不全是用于描述家族性颅缝早闭的术语,其中缝线受累通常包括颅顶、颅底和面部中部骨骼结构。颅面骨发育不全的综合征形式最初由卡彭特、阿佩尔、克鲁宗、塞特雷和乔岑、 Pfeiffer 等人描述。除了畸形的颅骨特征外,受影响个体的面部骨骼发育可能会有深刻改变。手术重建需要精心安排顺序和分阶段进行,要考虑个体的特定畸形、颅面生长模式和心理社会需求。颅面骨发育不全综合征的治疗是手术治疗,但重建各阶段的适应症、时机、类型和效果尚未得到充分评估,其艺术性和科学性一样强。本文回顾了颅面骨发育不全综合征的具体特征性临床特点,并介绍了目前重建分期的理念和基本原理。