LI Hong-Hua, HAO Yun-Peng, DU Lin, JIA Fei-Yong.
A case report of Apert syndrome[J]. Chinese Journal of Contemporary Pediatrics. 2011, 13(7): 604-605
中图分类号：
R596.1
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参考文献
［1］Herman TE, Siegel MJ. Apert syndrome with omphalocele［J］. J Perinatol, 2010, 30(10): 695-697.
［2］Soanca A, Dudea D, Gocan H, Roman A, Culic B. Oral manifestations in Apert syndrome: case presentation and a brief review of the literature［J］. Rom J Morphol Embryol, 2010, 51(3): 581584.
［3］Lolis MS, Bowe WP, Shalita AR. Acne and systemic disease［J］. Med Clin North Am, 2009, 93(6): 1161-1181.
［4］De D, Narang T, Kanwar AJ, Dogra S. Brachycephaly and syndactyly: Apert's syndrome［J］. Indian J Dermatol Venereol Leprol, 2008, 74(4):395-396.
［5］Slaney SF, Oldridge M, Hurst JA, Moriss-Kay GM, Hall CM, Poole MD, et al. Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome［J］. Am J Hum Genet, 1996, 58(5): 923-932.
［6］Holmes G, Rothschild G, Roy UB, Deng CX, Mansukhani A, Basilico C. Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology［J］. Dev Biol, 2009, 328(2): 273-284.
［7］Weber B, Schwabegger AH, Vodopiutz J, Janecke AR,Forstner R,Steiner H. Prenatal diagnosis of apert syndrome with cloverleaf skull deformity using ultrasound, fetal magnetic resonance imaging and genetic analysis［J］. Fetal Diagn Ther, 2010, 27(1): 51-56.
［8］Esparza J, Hinojosa J, García-Recuero I, Romance A, Pascual B, Martínez de Aragón A. Surgical treatment of isolated and syndromic craniosynostosis. Results and complications in 283 consecutive cases［J］.Neurocirugia (Astur), 2008, 19(6): 509-529.
［9］Gur I, Peled IJ, de Leon Falewski G, Meyer S. Rehabilitation aspects of Apert's syndrome［J］. Isr J Med Sci, 1984, 20(1): 50-54.
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