Prenatal Diagnosis of Agnathia-Otocephaly Using Sonography and Magnetic Resonance Imaging
Author:
Publisher
Wiley
Subject
Radiology, Nuclear Medicine and imaging,Radiological and Ultrasound Technology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.7863/ultra.32.8.1522/fullpdf
Reference10 articles.
1. Agnathia-otocephaly complex: report of three cases with involvement of two different Carnegie stages;Schiffer;Am J Med Genet,2002
2. PRRX1 is mutated in a fetus with agnathia-otocephaly;Sergi;Clin Genet,2011
3. Otocephaly: report of five new cases and a literature review;Faye-Petersen;Fetal Pediatr Pathol,2006
4. Familial agnathia-holoprosencephaly caused by an inherited unbalanced translocation and not autosomal recessive inheritance;Krassikoff;Am J Med Genet,1989
5. On the genetics of subnormal development of the head (otocephaly) in the guinea pig;Wright;Genetics,1934
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1. A case of rare isolated agnathia and literature review;American Journal of Medical Genetics Part A;2020-08-11
2. Agnathia-otocephaly complex: a case report and a literature review on recurrence risk;Case Reports in Perinatal Medicine;2020-01-01
3. The location of the fetal ears: A hint for prenatal diagnosis of agnathia‐otocephaly complex;Journal of Clinical Ultrasound;2019-02-12
4. Prenatal Diagnosis of Isolated Agnathia-Otocephaly: A Case Report and Review of the Literature;Case Reports in Obstetrics and Gynecology;2016
5. Severe Agnathia–Otocephaly Complex;Journal of Craniofacial Surgery;2015-11
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