Prenatal diagnosis of Apert syndrome using ultrasound, magnetic resonance imaging, and three-dimensional virtual/physical models: three case series and literature review
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/article/10.1007/s00381-018-3740-y/fulltext.html
Reference28 articles.
1. Tolarova MM, Harris JA, Ordway DE, Vargervik K (1997) Birth prevalence, mutation rate, sex ratio, parents’ age, and ethnicity in Apert syndrome. Am J Med Genet 72(4):394–398. https://doi.org/10.1002/(SICI)1096-8628(19971112)72:4<394::AID-AJMG4>3.0.CO;2-R
2. Cohen MM Jr, Kreiborg S, Lammer EJ, Cordero JF, Mastroiacovo P, Erickson JD, Roeper P, Martínez-Frías ML (1992) Birth prevalence study of the Apert syndrome. Am J Med Genet 42(5):655–659. https://doi.org/10.1002/ajmg.1320420505
3. Glaser RL, Broman KW, Schulman RL, Eskenazi B, Wyrobek AJ, Jabs EW (2003) The paternal-age effect in Apert syndrome is due, in part, to the increased frequency of mutations in sperm. Am J Hum Genet 73(4):939–947. https://doi.org/10.1086/378419
4. Helfer TM, Peixoto AB, Tonni G, Araujo Junior E (2016) Craniosynostosis: prenatal diagnosis by 2D/3D ultrasound, magnetic resonance imaging and computed tomography. Med Ultrason 18(3):378–385. https://doi.org/10.11152/mu.2013.2066.183.3du
5. Giancotti A, D’Ambrosio V, De Filippis A, Aliberti C, Pasquali G, Bernardo S, Manganaro L, PECRAM Study Group (2014) Comparison of ultrasound and magnetic resonance imaging in the prenatal diagnosis of Apert syndrome: report of a case. Childs Nerv Syst 30(8):1445–1448. https://doi.org/10.1007/s00381-014-2377-8
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