Neuropediatrics 2016; 47(01): 057-060
DOI: 10.1055/s-0035-1566447
Short Communication
Georg Thieme Verlag KG Stuttgart · New York

Severe and Progressive Fetal Ventriculomegaly Leading to the Diagnosis of Periventricular Nodular Heterotopias with Good Outcome

Joel Fluss
1   Pediatric Neurology, Pediatric Subspecialties Service, Geneva Children's Hospital, Switzerland
,
Jean-Marie Pellegrinelli
2   Department of Gynecology and Obstetrics, University Hospitals of Geneva, Geneva, Switzerland
,
Siv Fokstuen
3   Genetic Medicine, University Hospitals of Geneva, Switzerland
,
Marie-Laure Moutard
4   Pediatric Neurology, Hôpital d'Enfants Armand-Trousseau, Paris, France
,
Catherine Garel
5   Department of Pediatric Radiology, Hôpital d'Enfants Armand-Trousseau, Paris, France
,
Nadia Bahi-Buisson
6   Service de Neurologie pédiatrique, Hôpital Necker Enfants Malades, Paris, France
,
Marie-Hélène Bilieux
2   Department of Gynecology and Obstetrics, University Hospitals of Geneva, Geneva, Switzerland
,
Sylviane Hanquinet
7   Pediatric Radiology Unit, University of Geneva Children's Hospital, Switzerland
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Publikationsverlauf

17. Juni 2015

19. September 2015

Publikationsdatum:
16. November 2015 (online)

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Abstract

Severe fetal ventriculomegaly is generally associated with poor prognosis in terms of survival and neurodevelopment outcome. As such, many parents opt to terminate the pregnancy independently of a known etiology. We report here the case of a female fetus with severe progressive ventriculomegaly due to the unexpected presence of bilateral nodular periventricular heterotopias visualized on MRI of a fetal brain. Reaching a structural diagnosis was perceived as a relief for the parents and the pregnancy was continued. Neurodevelopment assessment at 3 years of age is normal with no epilepsy.