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孤立性透明隔缺如:产前诊断与结局。

Isolated absence of septum pellucidum: prenatal diagnosis and outcome.

机构信息

Unidad de Gestión Clínica de Genética, Reproducción y Medicina Fetal, Instituto de Biomedicina de Sevilla (IBIS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Sevilla, España.

出版信息

Fetal Diagn Ther. 2013;33(2):130-2. doi: 10.1159/000338009. Epub 2012 Apr 27.

Abstract

Septal agenesis is a rare cerebral developmental anomaly characterized by partial or complete absence of the septum pellucidum (ASP). Septal agenesis may be associated with various congenital brain malformations, namely holoprosencephaly, septooptic dysplasia (SOD), schizencephaly or agenesis of the corpus callosum. Current imaging technologies do not enable differentiation in utero between isolated ASP and SOD. This is due to the fact that optic nerve hypoplasia and endocrine anomalies are never ruled out completely. We report a case of prenatal diagnosis of isolated ASP based on 2D and 3D ultrasound and fetal MRI. Postnatal MRI confirmed prenatal findings and the boy is currently doing well at 18 months of age.

摘要

间隔发育不全是一种罕见的脑发育异常,其特征为透明隔(ASP)部分或完全缺失。间隔发育不全可能与各种先天性脑畸形有关,如全前脑、视隔发育不良(SOD)、脑裂畸形或胼胝体发育不全。目前的成像技术无法在子宫内区分孤立性 ASP 和 SOD。这是因为视神经发育不良和内分泌异常从未被完全排除。我们报告了一例基于二维和三维超声及胎儿 MRI 的孤立性 ASP 产前诊断病例。产后 MRI 证实了产前发现,该男孩目前 18 个月,情况良好。

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