Update on neuroimaging phenotypes of mid-hindbrain malformations

Purpose Neuroimaging techniques including structural magnetic resonance imaging (MRI) and functional positron emission tomography (PET) are useful in categorizing various midbrain-hindbrain (MHB) malformations, both in allowing diagnosis and in helping to understand the developmental processes that...

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Veröffentlicht in:Neuroradiology 2015-02, Vol.57 (2), p.113-138
Hauptverfasser: Jissendi-Tchofo, Patrice, Severino, Mariasavina, Nguema-Edzang, Béatrice, Toure, Cissé, Soto Ares, Gustavo, Barkovich, Anthony James
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Sprache:eng
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Zusammenfassung:Purpose Neuroimaging techniques including structural magnetic resonance imaging (MRI) and functional positron emission tomography (PET) are useful in categorizing various midbrain-hindbrain (MHB) malformations, both in allowing diagnosis and in helping to understand the developmental processes that were disturbed. Brain imaging phenotypes of numerous malformations are characteristic features that help in guiding the genetic testing in case of direct neuroimaging-genotype correlation or, at least, to differentiate among MHB malformations entities. The present review aims to provide the reader with an update of the use of neuroimaging applications in the fine analysis of MHB malformations, using a comprehensive, recently proposed developmental and genetic classification. Methods We have performed an extensive systematic review of the literature, from the embryology main steps of MHB development through the malformations entities, with regard to their molecular and genetic basis, conventional MRI features, and other neuroimaging characteristics. Results We discuss disorders in which imaging features are distinctive and how these features reflect the structural and functional impairment of the brain. Conclusion Recognition of specific MRI phenotypes, including advanced imaging features, is useful to recognize the MHB malformation entities, to suggest genetic investigations, and, eventually, to monitor the disease outcome after supportive therapies.
ISSN:0028-3940
1432-1920
DOI:10.1007/s00234-014-1431-2