1997
DOI: 10.1097/00006534-199704001-00030
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The Role of the Cranial Base in Facial Growth: Experimental Craniofacial Synostosis in the Rabbit

Abstract: Craniofacial synostosis designates premature fusion in sutures of the cranial vault (calvarium). When craniofacial synostosis is associated with a syndrome (e.g., Apert, Crouzon), premature fusion of the cranial base has been postulated to occur as well. This study was designed to determine whether the primary growth disturbance in craniofacial synostosis is located at the cranial base (i.e., spheno-occipital synchondrosis) or the calvarial vault (i.e., coronal and sagittal sutures) or both. Sixty newborn New … Show more

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Cited by 72 publications
(32 citation statements)
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“…This sample includes some classics as well as more modern work: Twitty (1932), Detwiler (1938), Washburn and Detwiler (1943), Moss (1961Moss ( , 1969Moss ( , 1997, Müller (1989), Müller and Streicher (1989), Burke (1991), Rosenberg et al (1997), Poikela et al (2000), Badyaev et al (2005), and Alaqeel et al (2006).…”
Section: Discontinuitiesmentioning
confidence: 99%
“…This sample includes some classics as well as more modern work: Twitty (1932), Detwiler (1938), Washburn and Detwiler (1943), Moss (1961Moss ( , 1969Moss ( , 1997, Müller (1989), Müller and Streicher (1989), Burke (1991), Rosenberg et al (1997), Poikela et al (2000), Badyaev et al (2005), and Alaqeel et al (2006).…”
Section: Discontinuitiesmentioning
confidence: 99%
“…7 Closure time is also sex-dependent, with girls fusing slightly earlier around age 12 and boys fusing slightly later around age 14. A key driver of cranial base and consequently facial growth, its premature fusion has been shown in animal models, 8 with circumstantial evidence in humans, 9 to be associated with both cranial base and midface hypoplasia. The purpose of this study was to review computed tomographic scans of Apert syndrome and Muenke syndrome patients to determine whether they had premature fusion of the sphenooccipital synchondrosis when compared with each other and to subjects without craniosynostosis syndromes and midface hypoplasia.…”
mentioning
confidence: 99%
“…In some cases, the cranial base anomalies are believed to be the primary cause of the overall abnormal craniofacial development (Kreiborg et al 1993). Consistent with this, animal study provides experimental evidence that cranial base fusion alone accounts for many craniofacial dysmorphic features (Rosenberg et al 1997). While most of the craniofacial skeletons are formed by intramembranous ossification, the cranial base is a site of endochondral ossification, a bone-forming process guided by a cartilage template.…”
Section: Introductionmentioning
confidence: 60%