KIAA0586中新的致病双等位基因变异扩展了纤毛病的变异谱。

IF 1.6
Yue Shen, Ruida He, Chao Lu, Ziheng Wang, Yufei Yu, Zongfu Cao, Minna Luo
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引用次数: 0

摘要

Joubert综合征(JBTS)是一组隐性神经发育障碍,被归类为具有遗传异质性的特定类型纤毛病。JBTS23是Joubert综合征的一种亚型,由KIAA0586基因变异引起。在这项研究中,我们报告了一个9个月大的男孩,根据中脑臼齿征和整体发育迟缓的存在,被诊断为JBTS。全外显子组测序鉴定出KIAA0586的两个致病变异(c.3944 T>G和c.3686 + 3A>G),符合常染色体隐性遗传模式。这些发现通过先证者及其父母的桑格测序得到了证实。本研究鉴定出KIAA0586的两个新的致病变异,为该患者提供了JBTS23的遗传学诊断,扩大了KIAA0586与JBTS相关的变异谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel Pathogenic Biallelic Variants in KIAA0586 Expand the Variant Spectrum of Ciliopathies.

Joubert syndrome (JBTS) is a group of recessive neurodevelopmental disorders classified as a specific type of ciliopathy with genetic heterogeneity. JBTS23, a subtype of Joubert syndrome, is caused by variations in the KIAA0586 gene. In this study, we report a 9-month-old boy diagnosed with JBTS based on the presence of the molar tooth sign in the midbrain and global developmental delay. Whole-exome sequencing identified two pathogenic variants in KIAA0586 (c.3944 T>G and c.3686 + 3A>G), consistent with an autosomal recessive inheritance pattern. These findings were confirmed through Sanger sequencing of the proband and his parents. This study identifies two novel pathogenic variants in KIAA0586, provides a genetic diagnosis for this patient as JBTS23, and expands the variant spectrum of KIAA0586 associated with JBTS.

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