Diagnosis of malformation of the cortical development in a monochorial twin pregnancy: case report
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URI: http://hdl.handle.net/10818/62197Visitar enlace: https://www.scopus.com/inward/ ...
ISSN: 0048766X
DOI: 10.24875/RECHOG.23000103
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Niño-Muriel J.M; Roncarati-Cannazzaro V; Aragón-Mendoza R.L; Russo-Vizcaino G.C; Calle-Bernal F.Date
2024Abstract
Introduction: Malformations of cortical development are the result from alterations in the neuroblast migration during the cerebral cortex formation. It's frequency in monochorial multiple pregnancies remains unknown. Objective: To report a case of monochorial multiple pregnancy with diagnosis of malformation of the cortical development in one of the fetuses. In addition, to review the literature regarding the diagnosis and prognosis of this entity. Method: A 19-year-old female with a monochorial diamniotic pregnancy of 26 weeks' gestation, arrived with an ultrasound anatomy scan visit, and fetal magnetic resonance imaging, we detected asymmetry in the cerebral hemispheres one of the fetuses, hypoplasia of the left sulcus of Sylvius with simplification of the gyrus pattern due to clusters of pachygyria and polymicrogyria. Those findings were confirmed afterbirth, with a definite diagnosis of neuronal migration disorder associated with vermian hypoplasia Results: Three cases of monochorial pregnancy with neuronal migration disorder with live newborn, common findings like microcephaly, lissencephaly and vermian hypoplasia. Conclusions: Prenatal diagnosis with neuronal migration disorder is done via ultrasound and magnetic resonance imaging. Neuronal migration disorders type II are the most common of them. Prognosis depends on the type of disorder; however, most patients have epileptiform activity and neurodevelopment impairment. © 2024 Sociedad Chilena de Obstetricia y Ginecologia. All rights reserved.
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Revista Chilena de Obstetricia y Ginecologia Vol. 89 N° 2
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- Facultad de Medicina [1345]