Literature DB >> 25463893

Agnathia-otocephaly: prenatal diagnosis by two- and three-dimensional ultrasound and magnetic resonance imaging. Case report.

Wagner Jou Hisaba1, Hérbene José Figuinha Milani1, Edward Araujo Júnior2, Jurandir Piassi Passos1, Enoch Quinderé Sá Barreto1, Natália Silva Carvalho1, Talita Micheletti Helfer1, David Batista Silva Pares1, Luciano Marcondes Machado Nardozza1, Antonio Fernandes Moron1.   

Abstract

A case of prenatally diagnosed otocephaly is reported. Otocephaly is an extremely rare malformation characterized by absence or hypoplasia of the mandible and abnormal horizontal position of the ears. 2D ultrasound performed at 25 weeks of gestation revealed agnathia, proboscis and hypotelorism. 3D ultrasound (rendering mode) and magnetic resonance imaging were used to evaluate the facial features, and were essential for characterization of facial malformations in otocephaly and for the demonstration and correct prenatal counseling of the couple.

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Year:  2014        PMID: 25463893     DOI: 10.11152/mu.201.3.2066.164.wjh1

Source DB:  PubMed          Journal:  Med Ultrason        ISSN: 1844-4172            Impact factor:   1.611


  1 in total

1.  Otocephaly: Agnathia- Microstomia-Synotia Syndrome- A Rare Congenital Anomaly.

Authors:  Sunil Vitthalrao Jagtap; Neerav Saini; Swati Jagtap; Sneha Saini
Journal:  J Clin Diagn Res       Date:  2015-09-01
  1 in total

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