By Mark P. Mooney, Michael I. Siegel
This accomplished textbook, edited via world-renowned specialists within the box, offers solutions to demanding situations within the analysis and therapy of craniofacial anomalies.The e-book integrates easy technological know-how and medical views, making a extra unified and useful “patient based” procedure. equipped in a logical, easy-to-follow constitution, this reference studies and provides state-of-the-art findings, masking the state-of-the-art in craniosynostosis and facial clefting from molecular, genetic, mobile, tissue, organismic, and populations degrees. utilizing standardized nomenclature and constant terminology, Understanding Craniofacial Anomalies comprises the recent explosion of development in learning genetic and epigenetic etiologies of syndromes, thereby delivering a special and holistic evaluate of this significant subject.
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Extra info for Understanding Craniofacial Anomalies: The Etiopathogenesis of Craniosynostoses and Facial Clefting
Example text
1989). LAHSHAL. A concise documentation system for cleft lip, alveolus, and palate diagnoses. In O. ), What Is a Cleft Lip and Palate? A Multidisciplinary Update (Stuttgart: Thieme), pp. 30–34. Lewin, M. , Croft, C. , and Shprintzen, R. J. (1980). Velopharyngeal insufficiency due to hypoplasia of the musculus uvulae and occult submucous cleft palate. Plast. Reconstr. Surg. 65, 585–591. Rollnick, B. , and Pruzansky, S. (1981). Genetic services at a center for craniofacial anomalies. Cleft Palate J.
Within these groups, it makes the most sense to refer to each individual structure by name. Within the primary palate are the lip and the maxillary alveolus, and the posterior palate contains the hard palate and the soft palate (or velum). Within each of these subgroupings, the following types of clefts may occur: complete, incomplete, and submucous. In addition, the primary palate and 21 the hard palate may be cleft unilaterally or bilaterally. ). There is no longer the need to use cryptic codes.
Smith’s Recognizable Patterns of Human Deformation (Philadelphia: W. B. Saunders). Graham, J. , and Smith, D. W. (1980). Coronal craniostenosis: fetal head constraint as one possible cause. Pediatrics 65, 995. Gripp, K. , McDonald-McGinn, D. , Whitaker, L. , Bartlett, S. , Glat, P. , Cassileth, L. , Zackai, E. , and Muenke, M. (1998). Identification of the first genetic cause of isolated unilateral coronal synostosis: a unique mutation in the fibroblast growth factor receptor 3 (FGFR3). J. Pediatr.