Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases

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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...

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Detalles Bibliográficos
Autores: Montenegro-Garreaud, Ximena, Hansen, 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.
Formato: artículo
Fecha de Publicación:2020
Institución:Universidad Peruana de Ciencias Aplicadas
Repositorio:UPC-Institucional
Lenguaje:inglés
OAI Identifier:oai:repositorioacademico.upc.edu.pe:10757/655505
Enlace del recurso:http://hdl.handle.net/10757/655505
Nivel de acceso:acceso embargado
Materia:data lake
genocentric
germline mosaicism
in-frame deletion
KIF1A
literature review
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oai_identifier_str oai:repositorioacademico.upc.edu.pe:10757/655505
network_acronym_str UUPC
network_name_str UPC-Institucional
repository_id_str 2670
dc.title.en_US.fl_str_mv Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases
title Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases
spellingShingle Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases
Montenegro-Garreaud, Ximena
data lake
genocentric
germline mosaicism
in-frame deletion
KIF1A
literature review
title_short Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases
title_full Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases
title_fullStr Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases
title_full_unstemmed Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases
title_sort Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases
author Montenegro-Garreaud, Ximena
author_facet Montenegro-Garreaud, Ximena
Hansen, 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.
author_role author
author2 Hansen, 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.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Montenegro-Garreaud, Ximena
Hansen, 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.
dc.subject.en_US.fl_str_mv data lake
genocentric
germline mosaicism
in-frame deletion
KIF1A
literature review
topic data lake
genocentric
germline mosaicism
in-frame deletion
KIF1A
literature review
description 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.
publishDate 2020
dc.date.accessioned.none.fl_str_mv 2021-04-14T12:28:39Z
dc.date.available.none.fl_str_mv 2021-04-14T12:28:39Z
dc.date.issued.fl_str_mv 2020-12-01
dc.type.en_US.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.issn.none.fl_str_mv 10597794
dc.identifier.doi.none.fl_str_mv 10.1002/humu.24118
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10757/655505
dc.identifier.eissn.none.fl_str_mv 10981004
dc.identifier.journal.en_US.fl_str_mv Human Mutation
dc.identifier.eid.none.fl_str_mv 2-s2.0-85092158304
dc.identifier.scopusid.none.fl_str_mv SCOPUS_ID:85092158304
dc.identifier.isni.none.fl_str_mv 0000 0001 2196 144X
identifier_str_mv 10597794
10.1002/humu.24118
10981004
Human Mutation
2-s2.0-85092158304
SCOPUS_ID:85092158304
0000 0001 2196 144X
url http://hdl.handle.net/10757/655505
dc.language.iso.en_US.fl_str_mv eng
language eng
dc.relation.url.en_US.fl_str_mv https://onlinelibrary.wiley.com/doi/10.1002/humu.24118
dc.rights.en_US.fl_str_mv info:eu-repo/semantics/embargoedAccess
eu_rights_str_mv embargoedAccess
dc.format.en_US.fl_str_mv application/pdf
dc.publisher.en_US.fl_str_mv John Wiley and Sons Inc
dc.source.es_PE.fl_str_mv Universidad Peruana de Ciencias Aplicadas (UPC)
Repositorio Academico - UPC
dc.source.none.fl_str_mv reponame:UPC-Institucional
instname:Universidad Peruana de Ciencias Aplicadas
instacron:UPC
instname_str Universidad Peruana de Ciencias Aplicadas
instacron_str UPC
institution UPC
reponame_str UPC-Institucional
collection UPC-Institucional
dc.source.journaltitle.none.fl_str_mv Human Mutation
dc.source.volume.none.fl_str_mv 41
dc.source.issue.none.fl_str_mv 12
dc.source.beginpage.none.fl_str_mv 2094
dc.source.endpage.none.fl_str_mv 2104
bitstream.url.fl_str_mv https://repositorioacademico.upc.edu.pe/bitstream/10757/655505/1/license.txt
bitstream.checksum.fl_str_mv 8a4605be74aa9ea9d79846c1fba20a33
bitstream.checksumAlgorithm.fl_str_mv MD5
repository.name.fl_str_mv Repositorio académico upc
repository.mail.fl_str_mv upc@openrepository.com
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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.National Institutes of HealthRevisión por paresapplication/pdfengJohn Wiley and Sons Inchttps://onlinelibrary.wiley.com/doi/10.1002/humu.24118info:eu-repo/semantics/embargoedAccessUniversidad Peruana de Ciencias Aplicadas (UPC)Repositorio Academico - UPCHuman Mutation411220942104reponame:UPC-Institucionalinstname:Universidad Peruana de Ciencias Aplicadasinstacron:UPCdata lakegenocentricgermline mosaicismin-frame deletionKIF1Aliterature reviewPhenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published casesinfo:eu-repo/semantics/articleLICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://repositorioacademico.upc.edu.pe/bitstream/10757/655505/1/license.txt8a4605be74aa9ea9d79846c1fba20a33MD51false10757/655505oai:repositorioacademico.upc.edu.pe:10757/6555052021-04-14 12:28:39.905Repositorio académico upcupc@openrepository.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