Literature DB >> 16260220

Application of the three-dimensional maximum mode in prenatal diagnosis of Apert syndrome.

Tilman Esser1, Patrick Rogalla, Christian Bamberg, Karim D Kalache.   

Abstract

Apert syndrome is a rare disorder characterized by coronal craniosynostosis, syndactyly, brachycephaly, midfacial hypoplasia, and central nervous system anomalies, among other malformations. We present a case of Apert syndrome examined at 22 + 0 weeks' gestation. Three-dimensional maximum mode was decisive for the correct prenatal diagnosis by demonstrating the cranial deformities.

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Year:  2005        PMID: 16260220     DOI: 10.1016/j.ajog.2005.07.043

Source DB:  PubMed          Journal:  Am J Obstet Gynecol        ISSN: 0002-9378            Impact factor:   8.661


  4 in total

1.  Comparison of ultrasound and magnetic resonance imaging in the prenatal diagnosis of Apert syndrome: report of a case.

Authors:  A Giancotti; V D'Ambrosio; A De Filippis; C Aliberti; G Pasquali; S Bernardo; L Manganaro
Journal:  Childs Nerv Syst       Date:  2014-02-25       Impact factor: 1.475

Review 2.  Prenatal diagnosis of Apert syndrome using ultrasound, magnetic resonance imaging, and three-dimensional virtual/physical models: three case series and literature review.

Authors:  Heron Werner; Pedro Castro; Pedro Daltro; Jorge Lopes; Gerson Ribeiro; Edward Araujo Júnior
Journal:  Childs Nerv Syst       Date:  2018-02-13       Impact factor: 1.475

3.  Acrocephalosyndactyly, Apert type, in a newborn: Cerebral sonography.

Authors:  C Poggiani; C Zambelloni; A Auriemma; A Colombo
Journal:  J Ultrasound       Date:  2007-07-26

Review 4.  Advances in evaluating the fetal skeleton.

Authors:  Ann-Edwidge Noel; Richard N Brown
Journal:  Int J Womens Health       Date:  2014-05-13
  4 in total

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