NSUN2型智力残疾综合征的眼部表现。

International journal of molecular epidemiology and genetics Pub Date : 2021-12-15 eCollection Date: 2021-01-01
Graham Pingree, Amy Harper, Jordan Snajczuk, Natario L Couser
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引用次数: 0

摘要

nsun2智力残疾综合征是一种罕见的细胞转录组紊乱,它阻止了适当的t-RNA剪接。这种疾病破坏细胞功能并导致RNA片段的积累,产生一系列症状,包括畸形相、张力低下、小头畸形和身材矮小。眼部表现有报道,但没有很好的特征。我们的研究提出了一个新病例,涉及一名4岁男孩,他患有新型NSUN2变异,其临床特征与该综合征一致。此外,通过系统回顾,我们讨论了24例先前报道的综合征,重点是眼睛和眼附件的临床特征。
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Eye manifestations in the NSUN2 intellectual disability syndrome.

The NSUN2-intellectual disability syndrome is a rare disorder of the cellular transcriptome that prevents proper t-RNA splicing. This disorder interrupts cellular function and leads to an accumulation of RNA fragments, producing a constellation of symptoms including dysmorphic facies, hypotonia, microcephaly, and short stature. Eye manifestations have been reported but not well characterized. Our study presents a new case involving a 4-year-old boy with novel NSUN2 variants and clinical features consistent with the syndrome. In addition, through a systemic review, we discuss the 24 previously reported cases of the syndrome with an emphasis on the eye and ocular adnexa clinical features.

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