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Prenatal Diagnosis of Frontonasal Dysplasia Associated With Bilateral Periventricular Nodular Heterotopia.

Authors :
Recio-Rodríguez, Manuel
Fernández-Mayoralas, Daniel Martín
Fernández-Jaén, Alberto
Fernández-Perrone, Ana Laura
Cano-Alonso, Raquel
Jiménez-de-La-Peña, Mar
Source :
Journal of Child Neurology; Oct2014, Vol. 29 Issue 10, pNP122-NP126, 1p
Publication Year :
2014

Abstract

Frontonasal dysplasia is an etiologically heterogeneous development alteration including a set of anomalies affecting the eyes, forehead, and nose as a result of a malformation of the frontonasal elevation. It could occur either in isolation or as part of a syndrome such as frontonasal dysplasia associated with periventricular heterotopia. Our goal is to document the first clinical case of prenatal diagnosis for frontonasal dysplasia associated with periventricular heterotopia by fetal magnetic resonance imaging (MRI) at weeks 19.5 and 29 and postnatal MRI. In conclusion, the presence of frontonasal dysplasia in a prenatal ultrasonography should always be followed by a fetal MRI with routine screening for periventricular nodular heterotopias so as to establish a more adequate prognosis for the family. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08830738
Volume :
29
Issue :
10
Database :
Complementary Index
Journal :
Journal of Child Neurology
Publication Type :
Academic Journal
Accession number :
98573465
Full Text :
https://doi.org/10.1177/0883073813508316