Literature DB >> 25297884

Apert syndrome: temporal lobe abnormalities on fetal brain imaging.

Zornitza Stark1, George McGillivray, Amanda Sampson, Ricardo Palma-Dias, Andrew Edwards, Joanne M Said, Gillian Whiteley, A Michelle Fink.   

Abstract

OBJECTIVES: Apert syndrome is characterized by craniosynostosis and complex hand and foot syndactyly, and an increased risk of brain, palate, heart, and visceral malformations, and intellectual disability. This study aims to describe the structural brain abnormalities detected by dedicated neuroimaging of fetuses with Apert syndrome.
METHODS: Retrospective review of ultrasound and magnetic resonance imaging brain imaging obtained in six fetuses with a diagnosis of Apert syndrome.
RESULTS: Five fetuses had attenuation of the septal leaflets, and two had corpus callosum dysgenesis. All six had temporal lobe expansion and overconvolution and temporal lobe clefts. The temporal lobe abnormalities preceded the development of cranial deformity in two fetuses.
CONCLUSION: Overexpansion and overconvolution of the temporal lobe is evident antenatally and is particularly conspicuous in the fetus when the normal brain is still relatively smooth (approximately 24 to 28 weeks of gestation).
© 2014 John Wiley & Sons, Ltd.

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Year:  2014        PMID: 25297884     DOI: 10.1002/pd.4515

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  8 in total

1.  Ultrasound and MR imaging findings in prenatal diagnosis of craniosynostosis syndromes.

Authors:  Eva I Rubio; Anna Blask; Dorothy I Bulas
Journal:  Pediatr Radiol       Date:  2016-02-25

2.  Fetal brain MRI in Apert syndrome: early in vivo detection of temporal lobe malformation.

Authors:  Miguel Quintas-Neves; João Paulo Soares-Fernandes
Journal:  Childs Nerv Syst       Date:  2018-06-28       Impact factor: 1.475

3.  Fetal magnetic resonance imaging of skeletal dysplasias.

Authors:  Leah A Gilligan; Maria A Calvo-Garcia; K Nicole Weaver; Beth M Kline-Fath
Journal:  Pediatr Radiol       Date:  2019-11-27

Review 4.  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

Review 5.  Fetal neuroimaging: an update on technical advances and clinical findings.

Authors:  Ashley J Robinson; M Ashraf Ederies
Journal:  Pediatr Radiol       Date:  2018-03-17

Review 6.  Apert syndrome: magnetic resonance imaging (MRI) of associated intracranial anomalies.

Authors:  Ai Peng Tan; Kshitij Mankad
Journal:  Childs Nerv Syst       Date:  2017-12-02       Impact factor: 1.475

7.  Differential diagnosis of syndromic craniosynostosis: a case series.

Authors:  Tamara Casteleyn; Denise Horn; Wolfgang Henrich; Stefan Verlohren
Journal:  Arch Gynecol Obstet       Date:  2021-10-11       Impact factor: 2.493

Review 8.  Definitions and classification of malformations of cortical development: practical guidelines.

Authors:  Mariasavina Severino; Ana Filipa Geraldo; Norbert Utz; Domenico Tortora; Ivana Pogledic; Wlodzimierz Klonowski; Fabio Triulzi; Filippo Arrigoni; Kshitij Mankad; Richard J Leventer; Grazia M S Mancini; James A Barkovich; Maarten H Lequin; Andrea Rossi
Journal:  Brain       Date:  2020-10-01       Impact factor: 13.501

  8 in total

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