BCL11B基因缺失与智力发育障碍伴语言迟缓、畸形相和t细胞异常1例报告

Q2 Medicine
Adriel Roa-Bautista, Mónica López-Duarte, Nerea Paz-Gandiaga, David San Segundo Arribas, J Gonzalo Ocejo-Vinyals
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引用次数: 0

摘要

在此,我们描述了一个13岁的女性患者面部畸形和免疫功能障碍引起的BCL11B基因突变的回顾性分析。体格检查时,患者表现出特殊的面部特征(细眉,小下颌骨,眼距变宽),语言和运动发育迟缓。补充检查显示CD8+扩增,2型先天淋巴样细胞缺失,IgG升高,T细胞分布改变。基因检测显示BCL11B基因外显子4存在杂合移码变异;c.1887_c。1893年delcggcggg (p.Gly630Glyfs * 91)。最后,BCL11B基因突变可导致神经系统和免疫系统发育异常,因此,有必要考虑以下临床和免疫表型患者的这种综合征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Deletion in the BCL11B Gene and Intellectual Developmental Disorder with Speech Delay, Dysmorphic Facies, and T-cell Abnormalities - a Case Report.

Deletion in the BCL11B Gene and Intellectual Developmental Disorder with Speech Delay, Dysmorphic Facies, and T-cell Abnormalities - a Case Report.

Deletion in the BCL11B Gene and Intellectual Developmental Disorder with Speech Delay, Dysmorphic Facies, and T-cell Abnormalities - a Case Report.

Herein we described a retrospective analysis of a 13-year-old female patient with facial dysmorphia and immune disorder caused by BCL11B gene mutation. The patient upon physical examination presented a particular face (thin eyebrows, small mandible, and widened eye distance), delayed language and motor development. Supplementary examination showed expansion of CD8+, absence of type 2 Innate Lymphoid Cells, increased IgG and altered distribution of T cells. Genetic testing revealed a heterozygous frameshift variation in exon 4 of the BCL11B gene; c.1887_c.1893delCGGCGGG (p.Gly630Glyfs*91). Finally, a BCL11B gene mutation could lead to abnormal development of the nervous and immune systems, therefore, it is necessary to consider this syndrome in patients with the clinical and immunological phenotype described below.

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