Two different prenatal imaging cerebral patterns of tubulinopathy

被引:15
作者
Cabet, S. [1 ,2 ]
Karl, K. [3 ,4 ]
Garel, C. [5 ]
Delius, M. [4 ]
Hartung, J. [6 ]
Lesca, G. [2 ]
Chaoui, R. [7 ]
Guibaud, L. [1 ]
机构
[1] Univ Claude Bernard Lyon 1, Hop Femme Mere Enfant, Imagerie Pediat & Foetale, 59 Blvd Pinel, F-69677 Lyon, France
[2] Univ Claude Bernard Lyon 1, Grp Hosp Est, Serv Genet, Lyon, France
[3] Ctr Prenatal Diag Munich, Munich, Germany
[4] Ludwig Maximilians Univ Munchen, Dept Obstet & Gynecol, Univ Hosp, Munich, Germany
[5] Hop Enfants Armand Trousseau, AP HP, Dept Pediat Imaging, Paris, France
[6] Off Prenatal Diag, Berlin, Germany
[7] Ctr Prenatal Diag & Human Genet, Berlin, Germany
关键词
asymmetric brainstem; distortion of interhemispheric fissure; prenatal imaging; TUBA1A gene; TUBB2B gene; TUBB3; gene; tubulinopathy;
D O I
10.1002/uog.22010
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
To illustrate the prenatal cerebral imaging features associated with tubulinopathy, we report on five affected fetuses from unrelated families, with a de-novo heterozygous variant in a tubulin gene (TUBA1A, TUBB2B or TUBB3). We identified two distinct prenatal imaging patterns related to tubulinopathy: a severe form, characterized by enlarged germinal matrices, microlissencephaly and a kinked brainstem; and a mild form which has not been reported previously in the prenatal literature. The latter form is associated with non-specific features, including an asymmetric brainstem, corpus callosal dysgenesis, a lack of Sylvian fissure operculization and distortion of the anterior part of the interhemispheric fissure with subsequent impacted medial borders of the frontal lobes, the combination of which, in the absence of additional extracerebral anomalies, is highly suggestive of tubulinopathy. Copyright (C) 2020 ISUOG. Published by John Wiley & Sons Ltd.
引用
收藏
页码:493 / 497
页数:5
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