Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases
Average rating
Cast your vote
You can rate an item by clicking the amount of stars they wish to award to this item.
When enough users have cast their vote on this item, the average rating will also be shown.
Star rating
Your vote was cast
Thank you for your feedback
Thank you for your feedback
Authors
Montenegro-Garreaud, XimenaHansen, Adam W.
Khayat, Michael M.
Chander, Varuna
Grochowski, Christopher M.
Jiang, Yunyun
Li, He
Mitani, Tadahiro
Kessler, Elena
Jayaseelan, Joy
Shen, Hua
Gezdirici, Alper
Pehlivan, Davut
Meng, Qingchang
Rosenfeld, Jill A.
Jhangiani, Shalini N.
Madan-Khetarpal, Suneeta
Scott, Daryl A.
Abarca-Barriga, Hugo
Trubnykova , Milana
Gingras, Marie Claude
Muzny, Donna M.
Posey, Jennifer E.
Liu, Pengfei
Lupski, James R.
Gibbs, Richard A.
Issue Date
2020-12-01
Metadata
Show full item recordPublisher
John Wiley and Sons IncJournal
Human MutationDOI
https://doi.org/10.1002/humu.24118Additional Links
https://onlinelibrary.wiley.com/doi/10.1002/humu.24118Abstract
KIF1A is a molecular motor for membrane-bound cargo important to the development and survival of sensory neurons. KIF1A dysfunction has been associated with several Mendelian disorders with a spectrum of overlapping phenotypes, ranging from spastic paraplegia to intellectual disability. We present a novel pathogenic in-frame deletion in the KIF1A molecular motor domain inherited by two affected siblings from an unaffected mother with apparent germline mosaicism. We identified eight additional cases with heterozygous, pathogenic KIF1A variants ascertained from a local data lake. Our data provide evidence for the expansion of KIF1A-associated phenotypes to include hip subluxation and dystonia as well as phenotypes observed in only a single case: gelastic cataplexy, coxa valga, and double collecting system. We review the literature and suggest that KIF1A dysfunction is better understood as a single neuromuscular disorder with variable involvement of other organ systems than a set of discrete disorders converging at a single locus.Type
info:eu-repo/semantics/articleRights
info:eu-repo/semantics/embargoedAccessLanguage
engISSN
10597794EISSN
10981004Sponsors
National Institutes of Healthae974a485f413a2113503eed53cd6c53
https://doi.org/10.1002/humu.24118
Scopus Count
Collections
