Prenatal diagnosis of non-typical Chiari malformation type I associated with de novo Nuclear Factor I A gene mutation: a case report

Abstract Background Chiari malformation is one of the most common Central nervous system (CNS) abnormalities that can be detected in routine fetal scanning. Chiari malformation type I (CMI) is a congenital defect characterized by a displacement of the cerebellar tonsils through the foramen magnum. T...

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Bibliographic Details

Published in:	Journal of Medical Case Reports
Main Authors:	Xuan-Hong Tomai, Huu-Trung Nguyen, Thanh-Truc Nguyen Thi, Tuan-Anh Nguyen, Thuy-Vy Nguyen
Format:	Article
Language:	English
Published:	BMC 2024-02-01
Subjects:	Case report Chiari malformation type I NFIA gene mutation Pregnancy Prenatal diagnosis
Online Access:	https://doi.org/10.1186/s13256-024-04361-1