Prenatal Diagnosis of Isolated Agnathia-Otocephaly: A Case Report and Review of the Literature
Author:
Affiliation:
1. The Jikei University School of Medicine, Nishishimbashi 25-83-3, Minato-ku, Tokyo 105-8461, Japan
2. National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo 157-8535, Japan
Abstract
Publisher
Hindawi Limited
Subject
Obstetrics and Gynecology
Link
http://downloads.hindawi.com/journals/criog/2016/8512351.pdf
Reference44 articles.
1. OTOCEPHALY: REPORT OF FIVE NEW CASES AND A LITERATURE REVIEW
2. Agnathia, situs inversus, and associated malformations
3. Current perspectives on the etiology of agnathia-otocephaly
4. Brains and faces in holoprosencephaly: pre- and postnatal description of 30 cases
5. Astomia-agnathia-holoprosencephaly association. Prenatal diagnosis of a new case
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1. Prenatal Diagnosis of Agnathia/Otocephaly: Associations and Outcomes-Large Case Series and Review of Literature;Journal of Fetal Medicine;2021-01-19
2. Otocephaly: Agnathia-Microstomia-Synotia Syndrome;International Journal of Infertility & Fetal Medicine;2021
3. A case of rare isolated agnathia and literature review;American Journal of Medical Genetics Part A;2020-08-11
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