Further evidence of involvement of ITSN1 in autosomal dominant neurodevelopmental disorder
- PMID: 38346866
- DOI: 10.1111/cge.14497
Further evidence of involvement of ITSN1 in autosomal dominant neurodevelopmental disorder
Abstract
A 5-year-old affected male had following phenotypes: autism, motor stereotypy, developmental regression, staring gaze, absent speech, and behavioral abnormality. The biochemical testing was normal and genetic testing identified a de novo pathogenic variant in ITSN1 gene in the proband. To our knowledge, this is the second report that elucidates the role of ITSN1 gene in an autosomal dominant neurodevelopmental disorder.
Keywords: ITSN1; autism spectrum disorder; autosomal dominant or de novo variants; rare disease.
© 2024 The Authors. Clinical Genetics published by John Wiley & Sons Ltd.
References
REFERENCES
-
- Bruel AL, Vitobello A, Thiffault I, et al. ITSN1: a novel candidate gene involved in autosomal dominant neurodevelopmental disorder spectrum. Eur J Hum Genet. 2022;30(1):111-116. doi:10.1038/s41431-021-00985-9
-
- Catalá-López F, Hutton B, Page MJ, et al. Mortality in persons with autism spectrum disorder or attention-deficit/hyperactivity disorder: a systematic review and meta-analysis. JAMA Pediatr. 2022;176(4):e216401. doi:10.1001/jamapediatrics.2021.6401
-
- Gryaznova T, Gubar O, Burdyniuk M, Kropyvko S, Rynditch A. WIP/ITSN1 complex is involved in cellular vesicle trafficking and formation of filopodia-like protrusions. Gene. 2018;674:49-56. doi:10.1016/j.gene.2018.06.078
-
- Yuen RKC, Merico D, Bookman M, et al. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder. Nat Neurosci. 2017;20(4):602-611. doi:10.1038/nn.4524
-
- Mosallaei M, Ehtesham N, Beheshtian M, et al. Phenotype and genotype spectrum of variants in guanine nucleotide exchange factor genes in a broad cohort of Iranian patients. Mol Genet Genomic Med. 2022;10(4):e1894. doi:10.1002/mgg3.1894
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
