A novel homozygous KY variant causing a complex neurological disorder.

TitleA novel homozygous KY variant causing a complex neurological disorder.
Publication TypeJournal Article
Year of Publication2020
AuthorsArif, B, Rasheed, A, Kumar, KR, Fatima, A, Abbas, G, Wohler, E, Sobriera, N, Lohmann, K, Naz, S
Corporate AuthorsBaylor-Hopkins Center for Mendelian Genomics
JournalEur J Med Genet
Volume63
Issue11
Pagination104031
Date Published2020 Nov
ISSN1878-0849
KeywordsChild, Female, Frameshift Mutation, Gait, Homozygote, Humans, Male, Myopathies, Structural, Congenital, Pedigree, Peptide Hydrolases, Phenotype, Spastic Paraplegia, Hereditary, Speech
Abstract

Mutations in the gene kyphoscoliosis peptidase (KY) are known to cause myofibrillar myopathy-7 and hereditary spastic paraplegia. We investigated the genetic cause of a complex neurological phenotype in a consanguineous Pakistani family with four affected members, manifesting lower limb spasticity and weakness, toe walking, pes equinovarus, and a speech disorder. Genome-wide linkage analysis with microsatellite markers delineated chromosome 3q22.2-q24 harboring the disease gene. Whole exome sequencing was performed for two subjects, identifying a homozygous 14-bp frameshift deletion NM_178554.6:c.842_855del; p(Val281GlyfsTer18) in KY. The variant segregated with the phenotype and was absent from public databases and 100 ethnically matched controls. We confirm a novel homozygous KY variant causing a complex neurological phenotype in this family. A review of previously reported KY variants suggests that variants in this gene can cause a spectrum of neurological phenotypes.

DOI10.1016/j.ejmg.2020.104031
Alternate JournalEur J Med Genet
PubMed ID32818658
PubMed Central IDPMC7554104
Grant ListU54 HG006542 / HG / NHGRI NIH HHS / United States