Back to Search Start Over

An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy

Authors :
Pagnamenta, Alistair T.
Kaiyrzhanov, Rauan
Zou, Yaqun
Da'as, Sahar, I
Maroofian, Reza
Donkervoort, Sandra
Dominik, Natalia
Lauffer, Marlen
Ferla, Matteo P.
Orioli, Andrea
Giess, Adam
Tucci, Arianna
Beetz, Christian
Sedghi, Maryam
Ansari, Behnaz
Barresi, Rita
Basiri, Keivan
Cortese, Andrea
Elgar, Greg
Fernandez-Garcia, Miguel A.
Yip, Janice
Foley, A. Reghan
Gutowski, Nicholas
Jungbluth, Heinz
Lassche, Saskia
Lavin, Tim
Marcelis, Carlo
Marks, Peter
Marini-Bettolo, Chiara
Medne, Livija
Moslemi, Ali-Reza
Sarkozy, Anna
Reilly, Mary M.
Muntoni, Francesco
Millan, Francisca
Muraresku, Colleen C.
Need, Anna C.
Nemeth, Andrea H.
Neuhaus, Sarah B.
Norwood, Fiona
O'Donnell, Marie
O'Driscoll, Mary
Rankin, Julia
Yum, Sabrina W.
Zolkipli-Cunningham, Zarazuela
Brusius, Isabell
Wunderlich, Gilbert
Karakaya, Mert
Wirth, Brunhilde
Fakhro, Khalid A.
Tajsharghi, Homa
Bonnemann, Carsten G.
Taylor, Jenny C.
Houlden, Henry
Pagnamenta, Alistair T.
Kaiyrzhanov, Rauan
Zou, Yaqun
Da'as, Sahar, I
Maroofian, Reza
Donkervoort, Sandra
Dominik, Natalia
Lauffer, Marlen
Ferla, Matteo P.
Orioli, Andrea
Giess, Adam
Tucci, Arianna
Beetz, Christian
Sedghi, Maryam
Ansari, Behnaz
Barresi, Rita
Basiri, Keivan
Cortese, Andrea
Elgar, Greg
Fernandez-Garcia, Miguel A.
Yip, Janice
Foley, A. Reghan
Gutowski, Nicholas
Jungbluth, Heinz
Lassche, Saskia
Lavin, Tim
Marcelis, Carlo
Marks, Peter
Marini-Bettolo, Chiara
Medne, Livija
Moslemi, Ali-Reza
Sarkozy, Anna
Reilly, Mary M.
Muntoni, Francesco
Millan, Francisca
Muraresku, Colleen C.
Need, Anna C.
Nemeth, Andrea H.
Neuhaus, Sarah B.
Norwood, Fiona
O'Donnell, Marie
O'Driscoll, Mary
Rankin, Julia
Yum, Sabrina W.
Zolkipli-Cunningham, Zarazuela
Brusius, Isabell
Wunderlich, Gilbert
Karakaya, Mert
Wirth, Brunhilde
Fakhro, Khalid A.
Tajsharghi, Homa
Bonnemann, Carsten G.
Taylor, Jenny C.
Houlden, Henry
Publication Year :
2021

Abstract

The extracellular matrix comprises a network of macromolecules such as collagens, proteoglycans and glycoproteins. VWA1 (von Willebrand factor A domain containing 1) encodes a component of the extracellular matrix that interacts with perlecan/collagen VI, appears to be involved in stabilizing extracellular matrix structures, and demonstrates high expression levels in tibial nerve. Vwa1-deficient mice manifest with abnormal peripheral nerve structure/function; however, VWA1 variants have not previously been associated with human disease. By interrogating the genome sequences of 74 180 individuals from the 100K Genomes Project in combination with international gene-matching efforts and targeted sequencing, we identified 17 individuals from 15 families with an autosomal-recessive, non-length dependent, hereditary motor neuropathy and rare biallelic variants in VWA1. A single disease-associated allele p.(G25Rfs*74), a 10-bp repeat expansion, was observed in 14/15 families and was homozygous in 10/15. Given an allele frequency in European populations approaching 1/1000, the seven unrelated homozygote individuals ascertained from the 100K Genomes Project represents a substantial enrichment above expected. Haplotype analysis identified a shared 220 kb region suggesting that this founder mutation arose 47000 years ago. A wide age-range of patients (6-83 years) helped delineate the clinical phenotype over time. The commonest disease presentation in the cohort was an early-onset (mean 2.0 +/- 1.4 years) non-length-dependent axonal hereditary motor neuropathy, confirmed on electrophysiology, which will have to be differentiated from other predominantly or pure motor neuropathies and neuronopathies. Because of slow disease progression, ambulation was largely preserved. Neurophysiology, muscle histopathology, and muscle MRI findings typically revealed clear neurogenic changes with single isolated cases displaying additional myopathic process. We speculate that a few findings of

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1312208036
Document Type :
Electronic Resource