Fetal Flat-Facies on Prenatal Ultrasound: Is it Chondrodysplasia Punctata? A Retrospective Chart Review of 62 Fetuses
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s40556-022-00334-w.pdf
Reference25 articles.
1. Blask AR, Rubio EI, Chapman KA, Lawrence AK, Bulas DI. Severe nasomaxillary hypoplasia (Binder phenotype) on prenatal US/MRI: an important marker for the prenatal diagnosis of chondrodysplasia punctata. Pediatr Radiol. 2018;48(7):979–91.
2. Quarrell OW, Koch M, Hughes HE. Maxillonasal dysplasia (Binder’s syndrome). J Med Genet. 1990;27(6):384–7.
3. Delaire J, Tessier P, Tulasne JF, Resche F. Clinical and radiologic aspects of maxillonasal dysostosis (Binder syndrome). Head Neck Surg. 1980;3(2):105–22.
4. Sheffield LJ, Danks DM, Mayne V, Hutchinson AL. Chondrodysplasia punctata-23 cases of a mild and relatively common variety. J Pediatr. 1976;89(6):916–23.
5. Oztürk H, Ipek A, Tan S, YenerÖztürk S, Keskin S, Kurt A, et al. Evaluation of fetal nasofrontal angle in the second trimester in normal pregnancies. J Clin Ultrasound JCU. 2011;39(1):18–20.
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