c.202_204del in NUP214 causes late onset form of febrile encephalopathy.
Sheeba FarooquiDhanya Lakshmi NarayananSelinda MascarenhasMichelle C do RosarioKarthik Vijay NairRadhakrishnan PeriyasamyAnju ShuklaPublished in: American journal of medical genetics. Part A (2024)
Nucleoporins (NUPs) are a group of transporter proteins that maintain homeostasis of nucleocytoplasmic transport of proteins and ribonucleic acids under physiological conditions. Biallelic pathogenic variants in NUP214 are known to cause susceptibility to acute infection-induced encephalopathy-9 (IIAE9, MIM#618426), which is characterized by severe and early-onset febrile encephalopathy causing neuroregression, developmental delay, microcephaly, epilepsy, ataxia, brain atrophy, and early death. NUP214-related IIAE9 has been reported in eight individuals from four distinct families till date. We identified a novel in-frame deletion, c.202_204del p.(Leu68del), in NUP214 by exome sequencing in a 20-year-old male with episodic ataxia, seizures, and encephalopathy, precipitated by febrile illness. Neuroimaging revealed progressive cerebellar atrophy. In silico predictions show a change in the protein conformation that may alter the downstream protein interactions with the NUP214 N-terminal region, probably impacting the mRNA export. We report this novel deletion in NUP214 as a cause for a late onset and less severe form of IIAE9.
Keyphrases
- early onset
- late onset
- urinary tract infection
- intellectual disability
- drug induced
- copy number
- single cell
- multiple sclerosis
- binding protein
- liver failure
- protein protein
- molecular docking
- chemotherapy induced
- amino acid
- white matter
- autism spectrum disorder
- small molecule
- cerebral ischemia
- extracorporeal membrane oxygenation
- blood brain barrier