| Literature DB >> 35126837 |
Graham Pingree1, Amy Harper2,3, Jordan Snajczuk4, Natario L Couser2,4,5.
Abstract
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. IJMEGEntities:
Keywords: 5-cytosine methyltransferase; NSUN2; NSUN2 intellectual disability syndrome; NSUN2-related syndrome; t-RNA modification
Year: 2021 PMID: 35126837 PMCID: PMC8784905
Source DB: PubMed Journal: Int J Mol Epidemiol Genet ISSN: 1948-1756