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前脑无裂畸形的中间半球变异型——表现为19周胎儿透明隔腔未显示及半球间囊肿

Middle Interhemispheric Variant of Holoprosencephaly - Presenting as Non-Visualized Cavum Septum Pellucidum and An Interhemispheric Cyst in A 19-Weeks Fetus.

作者信息

Vasudeva Akhila, Nayak Shalini S, Kadavigere Rajagopal, Girisha Katta M, Shetty Jyothi

机构信息

Associate Professor, Department of Obstetrics and Gynaecology, Kasturba Medical College, Manipal University , Manipal, India .

Junior Research Fellow, Department of Medical Genetics, Kasturba Medical College, Manipal University , Manipal, India .

出版信息

J Clin Diagn Res. 2015 Sep;9(9):QD11-3. doi: 10.7860/JCDR/2015/14076.6525. Epub 2015 Sep 1.

Abstract

Middle Interhemispheric variant (MIH) is a rare subtype of holoprosencephaly (HPE), also known as syntelencephaly. We present a case of MIH, which was diagnosed as an interhemispheric cyst on antenatal sonography at 19 weeks, but later diagnosed as MIH variant of holoprosencephaly after a postabortal MRI and perinatal autopsy.

摘要

中脑间叶变异型(MIH)是全前脑畸形(HPE)的一种罕见亚型,也称为融合性脑裂畸形。我们报告一例MIH病例,该病例在孕19周时产前超声检查诊断为脑间叶囊肿,但在流产后MRI及围产期尸检后诊断为全前脑畸形的MIH变异型。

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