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dc.contributor.authorEtchegaray, Adolfo.
dc.contributor.authorJuarez-Peñalva, Sofía.
dc.contributor.authorPetracchi, Florencia.
dc.contributor.authorEt al.
dc.date.accessioned2024-03-01T16:27:31Z
dc.date.available2024-03-01T16:27:31Z
dc.date.issued2020-08
dc.identifier.citationChilds Nerv Syst . 2020 Aug;36(8):1645-1660.es
dc.identifier.issn1433-0350
dc.identifier.urihttps://riu.austral.edu.ar/handle/123456789/3041
dc.descriptionDisponible en: https://link.springer.com/article/10.1007/s00381-020-04526-5es
dc.description.abstractAbstract Background: Fetal ventriculomegaly (VM) is a frequent finding in prenatal ultrasound. Rather than a proper diagnosis, VM is a sonographic sign, making prenatal counseling a complex and challenging undertaking. VM can range from severe pathologic processes leading to severe neurodevelopmental delay to normal variants. Discussion: A growing number of genetic conditions with different pathophysiological mechanisms, inheritance patterns, and long-term prognosis have been associated both to isolated and complex fetal VM. These include chromosomal abnormalities, copy number variants, and several single gene diseases. In this review, we describe some of the most common genetic conditions associated with fetal VM and provide a simplified diagnostic workflow for the clinician. Keywords: Congenital hydrocephalus; Fetal ventriculomegaly; Prenatal diagnosis; Prenatal genetic testing. PubMed Disclaimeres
dc.language.isoenes
dc.publisherSpringeres
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectCongenital hydrocephaluses
dc.subjectFetal ventriculomegalyes
dc.subjectPrenatal diagnosises
dc.titlePrenatal genetic considerations in congenital ventriculomegaly and hydrocephalus.es
dc.typeArticlees


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internacional