Three-dimensional computed tomography complements ultrasonography in prenatal diagnosis of Pfeiffer type 2 syndrome: a case report
Author:
Affiliation:
1. Department of Obstetrics and Gynecology, Fukushima Medical University School of Medicine
Publisher
Japan Society of Ultrasonics in Medicine
Subject
Radiology, Nuclear Medicine and imaging
Link
https://www.jstage.jst.go.jp/article/jjmu/50/4/50_JJMU.A.237/_pdf
Reference8 articles.
1. 1) Rai R, Iwanaga J, Dupont G, et al. Pfeiffer type 2 syndrome: review with updates on its genetics and molecular biology. Childs Nerv Syst. 2019;35:1451-5.
2. 2) Cohen MM Jr. Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis. Am J Med Genet. 1993;45:300-7.
3. 3) Giancotti A, D’Ambrosio V, Marchionni E, et al. Pfeiffer syndrome: literature review of prenatal sonographic findings and genetic diagnosis. J Matern Fetal Neonatal Med. 2017;30:2225-31.
4. 4) Macé G, Sonigo P, Cormier-Daire V, et al. Three-dimensional helical computed tomography in prenatal diagnosis of fetal skeletal dysplasia. Ultrasound Obstet Gynecol. 2013;42:161-8.
5. 5) Helfer TM, Peixoto AB, Tonni G, et al. Craniosynostosis: prenatal diagnosis by 2D/3D ultrasound, magnetic resonance imaging and computed tomography. Med Ultrason. 2016;18:378-85.
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