Prenatal Diagnosis of Lissencephaly Type 2 using Three-dimensional Ultrasound and Fetal MRI: Case Report and Review of the Literature
Abstract Lissencephaly is a genetic heterogeneous autosomal recessive disorder characterized by the classical triad: brain malformations, eye anomalies, and congenital muscular dystrophy. Prenatal diagnosis is feasible by demonstrating abnormal development of sulci and gyri. Magnetic resonance imagi...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Federação Brasileira das Sociedades de Ginecologia e Obstetrícia
2016-04-01
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Series: | Revista Brasileira de Ginecologia e Obstetrícia |
Subjects: | |
Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-72032016000400201&tlng=en |