The goal of the Center for Craniofacial Development and Disorders is to increase our understanding of normal and abnormal craniofacial development, promote prevention of craniofacial disease, and improve diagnosis and treatment of craniofacial disorders, including oral and dental conditions. Craniofacial abnormalities compose a large and heterogeneous group of human malformations. Of the over 5000 known human genetic syndromes, over 700 have craniofacial abnormalities. Oral clefting and craniosynostosis are among the most common malformations in humans and present a major health issue because of their associated medical, surgical, and psychological implications. To advance our knowledge, the Center will study the normal process of craniofacial development and the pathogenesis of craniosynostosis, oral clefting, and other craniofacial disorders in zebrafish, mice, rabbits, and humans from the phenotypic to the molecular level using a multi-disciplinary interactive approach. The Center will include the Administrative, Clinical, Animal, Molecular/Technology, Biostatistical, and Education/Informatics Cores which will support eight projects encompassing: 1) basic science, 2) clinical research, 3) behavioral and social sciences and health services, 4) environmental sciences, 5) technology development and liaison with industry, 6) demonstration and outreach programs, and 7) education and training for scientists, health care professionals, patients, and the public. Projects I and II will use zebrafish as a model organisms to study retinoic and ethanol effects of the morphogenesis of cranial neural crest cells, and mouse as a model organism to study the molecular pathogenesis of ethanol-induced craniofacial malformations and cell death. Projects III, IV, V, and VI will study morphologic aspects of the facial tissues, skull, and brain, developmental processes, molecular biology, genetics, and treatment of craniosynostosis in rabbits, mice, and humans. Projects VII and VIII will identify susceptibility genes for oral clefting and will analyze behavioral aspects and quantify of life for patients with non-syndromic oral clefting and craniosynostosis. The Center will be based at Johns Hopkins University with collaborative ties both nationally and internationally, with participants in 14 states and seven other countries.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Comprehensive Center (P60)
Project #
1P60DE013078-01
Application #
2800214
Study Section
Special Emphasis Panel (ZDE1-YS (10))
Project Start
1999-08-01
Project End
2004-07-31
Budget Start
1999-08-01
Budget End
2000-07-31
Support Year
1
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Pediatrics
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Richtsmeier, Joan T (2018) A century of development. Am J Phys Anthropol 165:726-740
Taub, Margaret A; Schwender, Holger; Beaty, Terri H et al. (2012) Incorporating genotype uncertainties into the genotypic TDT for main effects and gene-environment interactions. Genet Epidemiol 36:225-34
Ludwig, Kerstin U; Mangold, Elisabeth; Herms, Stefan et al. (2012) Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. Nat Genet 44:968-71
Hill, Cheryl A; Vaddi, S; Moffitt, Amanda et al. (2011) Intracranial volume and whole brain volume in infants with unicoronal craniosynostosis. Cleft Palate Craniofac J 48:394-8
Aldridge, Kristina (2011) Patterns of differences in brain morphology in humans as compared to extant apes. J Hum Evol 60:94-105
Richtsmeier, J T; Deleon, V B (2009) Morphological integration of the skull in craniofacial anomalies. Orthod Craniofac Res 12:149-58
Frazier, Brenda C; Mooney, Mark P; Losken, H Wolfgang et al. (2008) Comparison of craniofacial phenotype in craniosynostotic rabbits treated with anti-Tgf-beta2 at suturectomy site. Cleft Palate Craniofac J 45:571-82
Mooney, Mark P; Losken, H Wolfgang; Moursi, Amr M et al. (2007) Anti-TGF-beta2 antibody therapy inhibits postoperative resynostosis in craniosynostotic rabbits. Plast Reconstr Surg 119:1200-12;discussion 1213-5
Park, Ji Wan; McIntosh, Iain; Hetmanski, Jacqueline B et al. (2007) Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations. Genet Med 9:219-27
Parsons, Trish; Ryan, Timothy M; Reeves, Roger H et al. (2007) Microstructure of trabecular bone in a mouse model for Down syndrome. Anat Rec (Hoboken) 290:414-21

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