Title | A novel homozygous KY variant causing a complex neurological disorder. |
Publication Type | Journal Article |
Year of Publication | 2020 |
Authors | Arif, B, Rasheed, A, Kumar, KR, Fatima, A, Abbas, G, Wohler, E, Sobriera, N, Lohmann, K, Naz, S |
Corporate Authors | Baylor-Hopkins Center for Mendelian Genomics |
Journal | Eur J Med Genet |
Volume | 63 |
Issue | 11 |
Pagination | 104031 |
Date Published | 2020 Nov |
ISSN | 1878-0849 |
Keywords | Child, 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. |
DOI | 10.1016/j.ejmg.2020.104031 |
Alternate Journal | Eur J Med Genet |
PubMed ID | 32818658 |
PubMed Central ID | PMC7554104 |
Grant List | U54 HG006542 / HG / NHGRI NIH HHS / United States |