| Literature DB >> 35099671 |
Julia Macintosh1,2, Alexa Derksen1,2, Chantal Poulin1,3,4, Nancy Braverman2,3,5,6, Adeline Vanderver7,8, Isabelle Thiffault9,10,11, Steffen Albrecht12, Geneviève Bernard13,14,15,16,17.
Abstract
Negative regulator of reactive oxygen species (NRROS) is a leucine-rich repeat protein expressed by microglia and perivascular macrophages. To date, 9 individuals have been reported with biallelic NRROS variants. Here, we report one individual with a severe neurodegenerative phenotype in which exome sequencing identified 2 novel variants in NRROS, a missense variant (c.185T>C, p.Leu62Pro) and a premature stop codon (c.310C>T, p.Gln104Ter). Pathological examination revealed both extensive grey and white matter involvement, dystrophic calcifications, and infiltration of foamy macrophages. This is the first reported case of NRROS variants with a mitochondrial ultrastructure abnormality noted on electron microscopy analysis of post-mortem tissue.Entities:
Keywords: Exome sequencing; Intracranial calcifications; NRROS; Pediatric neurodegeneration
Mesh:
Year: 2022 PMID: 35099671 PMCID: PMC9289721 DOI: 10.1007/s10048-022-00683-8
Source DB: PubMed Journal: Neurogenetics ISSN: 1364-6745 Impact factor: 3.017