TELO2‐related syndrome (You‐Hoover‐Fong syndrome): Description of 14 new affected individuals and review of the literature
You‐Hoover‐Fong syndrome (YHFS) is an autosomal recessive condition caused by pathogenic variants in the TELO2 gene. Affected individuals were reported to have global developmental delay, intellectual disability, microcephaly, dysmorphic facial features, ocular involvement including cortical visual...
Gespeichert in:
Veröffentlicht in: | American journal of medical genetics. Part A 2023-05, Vol.191 (5), p.1261-1272 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1272 |
---|---|
container_issue | 5 |
container_start_page | 1261 |
container_title | American journal of medical genetics. Part A |
container_volume | 191 |
creator | Albokhari, Daniah Pritchard, Amanda Barone Beil, Adelyn Muss, Candace Bupp, Caleb Grange, Dorothy K. Delplancq, Geoffroy Heeley, Jennifer Zuteck, Melissa Morrow, Michelle M. Kuentz, Paul Palculict, Timothy Blake Hoover‐Fong, Julie E. |
description | You‐Hoover‐Fong syndrome (YHFS) is an autosomal recessive condition caused by pathogenic variants in the TELO2 gene. Affected individuals were reported to have global developmental delay, intellectual disability, microcephaly, dysmorphic facial features, ocular involvement including cortical visual impairment, strabismus, cataract and rotatory nystagmus, movement disorder, hypertonia and spasticity, balance disturbance and ataxia, and abnormal sleep pattern. Other features reported include poor growth, cleft palate, cardiac malformations, epilepsy, scoliosis, and hearing loss. To date, 12 individuals with YHFS have been reported in the literature. Here we describe 14 new individuals with YHFS from 10 families. Their clinical presentation provides additional support of the phenotype recognized previously and delineates the clinical spectrum associated with YHFS syndrome. In addition, we present a review of the literature including follow‐up data on four previously reported individuals with YHFS. |
doi_str_mv | 10.1002/ajmg.a.63142 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2798713276</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2796869654</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4022-3eac94475f20a1739f8d9112d54fb2cdad3d3c55b866a8869d75047800f4ce3a3</originalsourceid><addsrcrecordid>eNp90ctuEzEUBuARAtHSsmONLLEpEkl99wy7qPQCStVNu2BlOfZxcTQzTu2ZVNn1EXhGngSHlCxYsPKRz6dfR_qr6h3BU4IxPTXL7n5qppIRTl9Uh0QIOuE1Yy_3MxUH1ZuclxgzLJR8XR0wqRolCDusnm7P5zf019PPBK0ZwKG86V2KHaCT73Es_1cxriGV4SL29_vtx8_oC2SbwmoIsUfRI8JRD4_IeA92mxN6F9bBjabNyPQOJViHsi9y-AGoDQMkM4wJjqtXvhh4-_weVXcX57dnV5P5zeXXs9l8YjmmdMLA2IZzJTzFhijW-No1hFAnuF9Q64xjjlkhFrWUpq5l45TAXNUYe26BGXZUnexyVyk-jJAH3YVsoW1ND3HMmqqmVoRRJQv98A9dxjH15bqtkiVcCl7Up52yKeacwOtVCp1JG02w3jajt81oo_80U_j759Bx0YHb479VFMB34DG0sPlvmJ59u76c7XJ_A7eenOY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2796869654</pqid></control><display><type>article</type><title>TELO2‐related syndrome (You‐Hoover‐Fong syndrome): Description of 14 new affected individuals and review of the literature</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Albokhari, Daniah ; Pritchard, Amanda Barone ; Beil, Adelyn ; Muss, Candace ; Bupp, Caleb ; Grange, Dorothy K. ; Delplancq, Geoffroy ; Heeley, Jennifer ; Zuteck, Melissa ; Morrow, Michelle M. ; Kuentz, Paul ; Palculict, Timothy Blake ; Hoover‐Fong, Julie E.</creator><creatorcontrib>Albokhari, Daniah ; Pritchard, Amanda Barone ; Beil, Adelyn ; Muss, Candace ; Bupp, Caleb ; Grange, Dorothy K. ; Delplancq, Geoffroy ; Heeley, Jennifer ; Zuteck, Melissa ; Morrow, Michelle M. ; Kuentz, Paul ; Palculict, Timothy Blake ; Hoover‐Fong, Julie E.</creatorcontrib><description>You‐Hoover‐Fong syndrome (YHFS) is an autosomal recessive condition caused by pathogenic variants in the TELO2 gene. Affected individuals were reported to have global developmental delay, intellectual disability, microcephaly, dysmorphic facial features, ocular involvement including cortical visual impairment, strabismus, cataract and rotatory nystagmus, movement disorder, hypertonia and spasticity, balance disturbance and ataxia, and abnormal sleep pattern. Other features reported include poor growth, cleft palate, cardiac malformations, epilepsy, scoliosis, and hearing loss. To date, 12 individuals with YHFS have been reported in the literature. Here we describe 14 new individuals with YHFS from 10 families. Their clinical presentation provides additional support of the phenotype recognized previously and delineates the clinical spectrum associated with YHFS syndrome. In addition, we present a review of the literature including follow‐up data on four previously reported individuals with YHFS.</description><identifier>ISSN: 1552-4825</identifier><identifier>EISSN: 1552-4833</identifier><identifier>DOI: 10.1002/ajmg.a.63142</identifier><identifier>PMID: 36797513</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Ataxia ; Brain Diseases - complications ; Cleft lip/palate ; developmental delay ; Epilepsy ; Epilepsy - complications ; Hearing loss ; Humans ; Intellectual disabilities ; Intellectual Disability - pathology ; Literature reviews ; microcephaly ; Microcephaly - pathology ; Microencephaly ; Phenotypes ; Scoliosis ; Spasticity ; Strabismus ; Syndrome ; syndromic intellectual disabilities ; TELO2 ; YHFS ; You‐Hoover‐Fong syndrome</subject><ispartof>American journal of medical genetics. Part A, 2023-05, Vol.191 (5), p.1261-1272</ispartof><rights>2023 The Authors. published by Wiley Periodicals LLC.</rights><rights>2023 The Authors. American Journal of Medical Genetics Part A published by Wiley Periodicals LLC.</rights><rights>2023. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4022-3eac94475f20a1739f8d9112d54fb2cdad3d3c55b866a8869d75047800f4ce3a3</citedby><cites>FETCH-LOGICAL-c4022-3eac94475f20a1739f8d9112d54fb2cdad3d3c55b866a8869d75047800f4ce3a3</cites><orcidid>0000-0001-7150-4917 ; 0000-0003-2814-6303 ; 0000-0001-7425-6322 ; 0000-0002-0691-8985 ; 0000-0003-4255-0396 ; 0000-0001-9475-0934 ; 0000-0003-2114-8066 ; 0000-0002-9189-6847 ; 0000-0001-7380-0760 ; 0000-0002-1242-5626</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fajmg.a.63142$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fajmg.a.63142$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36797513$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Albokhari, Daniah</creatorcontrib><creatorcontrib>Pritchard, Amanda Barone</creatorcontrib><creatorcontrib>Beil, Adelyn</creatorcontrib><creatorcontrib>Muss, Candace</creatorcontrib><creatorcontrib>Bupp, Caleb</creatorcontrib><creatorcontrib>Grange, Dorothy K.</creatorcontrib><creatorcontrib>Delplancq, Geoffroy</creatorcontrib><creatorcontrib>Heeley, Jennifer</creatorcontrib><creatorcontrib>Zuteck, Melissa</creatorcontrib><creatorcontrib>Morrow, Michelle M.</creatorcontrib><creatorcontrib>Kuentz, Paul</creatorcontrib><creatorcontrib>Palculict, Timothy Blake</creatorcontrib><creatorcontrib>Hoover‐Fong, Julie E.</creatorcontrib><title>TELO2‐related syndrome (You‐Hoover‐Fong syndrome): Description of 14 new affected individuals and review of the literature</title><title>American journal of medical genetics. Part A</title><addtitle>Am J Med Genet A</addtitle><description>You‐Hoover‐Fong syndrome (YHFS) is an autosomal recessive condition caused by pathogenic variants in the TELO2 gene. Affected individuals were reported to have global developmental delay, intellectual disability, microcephaly, dysmorphic facial features, ocular involvement including cortical visual impairment, strabismus, cataract and rotatory nystagmus, movement disorder, hypertonia and spasticity, balance disturbance and ataxia, and abnormal sleep pattern. Other features reported include poor growth, cleft palate, cardiac malformations, epilepsy, scoliosis, and hearing loss. To date, 12 individuals with YHFS have been reported in the literature. Here we describe 14 new individuals with YHFS from 10 families. Their clinical presentation provides additional support of the phenotype recognized previously and delineates the clinical spectrum associated with YHFS syndrome. In addition, we present a review of the literature including follow‐up data on four previously reported individuals with YHFS.</description><subject>Ataxia</subject><subject>Brain Diseases - complications</subject><subject>Cleft lip/palate</subject><subject>developmental delay</subject><subject>Epilepsy</subject><subject>Epilepsy - complications</subject><subject>Hearing loss</subject><subject>Humans</subject><subject>Intellectual disabilities</subject><subject>Intellectual Disability - pathology</subject><subject>Literature reviews</subject><subject>microcephaly</subject><subject>Microcephaly - pathology</subject><subject>Microencephaly</subject><subject>Phenotypes</subject><subject>Scoliosis</subject><subject>Spasticity</subject><subject>Strabismus</subject><subject>Syndrome</subject><subject>syndromic intellectual disabilities</subject><subject>TELO2</subject><subject>YHFS</subject><subject>You‐Hoover‐Fong syndrome</subject><issn>1552-4825</issn><issn>1552-4833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNp90ctuEzEUBuARAtHSsmONLLEpEkl99wy7qPQCStVNu2BlOfZxcTQzTu2ZVNn1EXhGngSHlCxYsPKRz6dfR_qr6h3BU4IxPTXL7n5qppIRTl9Uh0QIOuE1Yy_3MxUH1ZuclxgzLJR8XR0wqRolCDusnm7P5zf019PPBK0ZwKG86V2KHaCT73Es_1cxriGV4SL29_vtx8_oC2SbwmoIsUfRI8JRD4_IeA92mxN6F9bBjabNyPQOJViHsi9y-AGoDQMkM4wJjqtXvhh4-_weVXcX57dnV5P5zeXXs9l8YjmmdMLA2IZzJTzFhijW-No1hFAnuF9Q64xjjlkhFrWUpq5l45TAXNUYe26BGXZUnexyVyk-jJAH3YVsoW1ND3HMmqqmVoRRJQv98A9dxjH15bqtkiVcCl7Up52yKeacwOtVCp1JG02w3jajt81oo_80U_j759Bx0YHb479VFMB34DG0sPlvmJ59u76c7XJ_A7eenOY</recordid><startdate>202305</startdate><enddate>202305</enddate><creator>Albokhari, Daniah</creator><creator>Pritchard, Amanda Barone</creator><creator>Beil, Adelyn</creator><creator>Muss, Candace</creator><creator>Bupp, Caleb</creator><creator>Grange, Dorothy K.</creator><creator>Delplancq, Geoffroy</creator><creator>Heeley, Jennifer</creator><creator>Zuteck, Melissa</creator><creator>Morrow, Michelle M.</creator><creator>Kuentz, Paul</creator><creator>Palculict, Timothy Blake</creator><creator>Hoover‐Fong, Julie E.</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7150-4917</orcidid><orcidid>https://orcid.org/0000-0003-2814-6303</orcidid><orcidid>https://orcid.org/0000-0001-7425-6322</orcidid><orcidid>https://orcid.org/0000-0002-0691-8985</orcidid><orcidid>https://orcid.org/0000-0003-4255-0396</orcidid><orcidid>https://orcid.org/0000-0001-9475-0934</orcidid><orcidid>https://orcid.org/0000-0003-2114-8066</orcidid><orcidid>https://orcid.org/0000-0002-9189-6847</orcidid><orcidid>https://orcid.org/0000-0001-7380-0760</orcidid><orcidid>https://orcid.org/0000-0002-1242-5626</orcidid></search><sort><creationdate>202305</creationdate><title>TELO2‐related syndrome (You‐Hoover‐Fong syndrome): Description of 14 new affected individuals and review of the literature</title><author>Albokhari, Daniah ; Pritchard, Amanda Barone ; Beil, Adelyn ; Muss, Candace ; Bupp, Caleb ; Grange, Dorothy K. ; Delplancq, Geoffroy ; Heeley, Jennifer ; Zuteck, Melissa ; Morrow, Michelle M. ; Kuentz, Paul ; Palculict, Timothy Blake ; Hoover‐Fong, Julie E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4022-3eac94475f20a1739f8d9112d54fb2cdad3d3c55b866a8869d75047800f4ce3a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Ataxia</topic><topic>Brain Diseases - complications</topic><topic>Cleft lip/palate</topic><topic>developmental delay</topic><topic>Epilepsy</topic><topic>Epilepsy - complications</topic><topic>Hearing loss</topic><topic>Humans</topic><topic>Intellectual disabilities</topic><topic>Intellectual Disability - pathology</topic><topic>Literature reviews</topic><topic>microcephaly</topic><topic>Microcephaly - pathology</topic><topic>Microencephaly</topic><topic>Phenotypes</topic><topic>Scoliosis</topic><topic>Spasticity</topic><topic>Strabismus</topic><topic>Syndrome</topic><topic>syndromic intellectual disabilities</topic><topic>TELO2</topic><topic>YHFS</topic><topic>You‐Hoover‐Fong syndrome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Albokhari, Daniah</creatorcontrib><creatorcontrib>Pritchard, Amanda Barone</creatorcontrib><creatorcontrib>Beil, Adelyn</creatorcontrib><creatorcontrib>Muss, Candace</creatorcontrib><creatorcontrib>Bupp, Caleb</creatorcontrib><creatorcontrib>Grange, Dorothy K.</creatorcontrib><creatorcontrib>Delplancq, Geoffroy</creatorcontrib><creatorcontrib>Heeley, Jennifer</creatorcontrib><creatorcontrib>Zuteck, Melissa</creatorcontrib><creatorcontrib>Morrow, Michelle M.</creatorcontrib><creatorcontrib>Kuentz, Paul</creatorcontrib><creatorcontrib>Palculict, Timothy Blake</creatorcontrib><creatorcontrib>Hoover‐Fong, Julie E.</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of medical genetics. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Albokhari, Daniah</au><au>Pritchard, Amanda Barone</au><au>Beil, Adelyn</au><au>Muss, Candace</au><au>Bupp, Caleb</au><au>Grange, Dorothy K.</au><au>Delplancq, Geoffroy</au><au>Heeley, Jennifer</au><au>Zuteck, Melissa</au><au>Morrow, Michelle M.</au><au>Kuentz, Paul</au><au>Palculict, Timothy Blake</au><au>Hoover‐Fong, Julie E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>TELO2‐related syndrome (You‐Hoover‐Fong syndrome): Description of 14 new affected individuals and review of the literature</atitle><jtitle>American journal of medical genetics. Part A</jtitle><addtitle>Am J Med Genet A</addtitle><date>2023-05</date><risdate>2023</risdate><volume>191</volume><issue>5</issue><spage>1261</spage><epage>1272</epage><pages>1261-1272</pages><issn>1552-4825</issn><eissn>1552-4833</eissn><abstract>You‐Hoover‐Fong syndrome (YHFS) is an autosomal recessive condition caused by pathogenic variants in the TELO2 gene. Affected individuals were reported to have global developmental delay, intellectual disability, microcephaly, dysmorphic facial features, ocular involvement including cortical visual impairment, strabismus, cataract and rotatory nystagmus, movement disorder, hypertonia and spasticity, balance disturbance and ataxia, and abnormal sleep pattern. Other features reported include poor growth, cleft palate, cardiac malformations, epilepsy, scoliosis, and hearing loss. To date, 12 individuals with YHFS have been reported in the literature. Here we describe 14 new individuals with YHFS from 10 families. Their clinical presentation provides additional support of the phenotype recognized previously and delineates the clinical spectrum associated with YHFS syndrome. In addition, we present a review of the literature including follow‐up data on four previously reported individuals with YHFS.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>36797513</pmid><doi>10.1002/ajmg.a.63142</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-7150-4917</orcidid><orcidid>https://orcid.org/0000-0003-2814-6303</orcidid><orcidid>https://orcid.org/0000-0001-7425-6322</orcidid><orcidid>https://orcid.org/0000-0002-0691-8985</orcidid><orcidid>https://orcid.org/0000-0003-4255-0396</orcidid><orcidid>https://orcid.org/0000-0001-9475-0934</orcidid><orcidid>https://orcid.org/0000-0003-2114-8066</orcidid><orcidid>https://orcid.org/0000-0002-9189-6847</orcidid><orcidid>https://orcid.org/0000-0001-7380-0760</orcidid><orcidid>https://orcid.org/0000-0002-1242-5626</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1552-4825 |
ispartof | American journal of medical genetics. Part A, 2023-05, Vol.191 (5), p.1261-1272 |
issn | 1552-4825 1552-4833 |
language | eng |
recordid | cdi_proquest_miscellaneous_2798713276 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Ataxia Brain Diseases - complications Cleft lip/palate developmental delay Epilepsy Epilepsy - complications Hearing loss Humans Intellectual disabilities Intellectual Disability - pathology Literature reviews microcephaly Microcephaly - pathology Microencephaly Phenotypes Scoliosis Spasticity Strabismus Syndrome syndromic intellectual disabilities TELO2 YHFS You‐Hoover‐Fong syndrome |
title | TELO2‐related syndrome (You‐Hoover‐Fong syndrome): Description of 14 new affected individuals and review of the literature |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T23%3A17%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=TELO2%E2%80%90related%20syndrome%20(You%E2%80%90Hoover%E2%80%90Fong%20syndrome):%20Description%20of%2014%20new%20affected%20individuals%20and%20review%20of%20the%20literature&rft.jtitle=American%20journal%20of%20medical%20genetics.%20Part%20A&rft.au=Albokhari,%20Daniah&rft.date=2023-05&rft.volume=191&rft.issue=5&rft.spage=1261&rft.epage=1272&rft.pages=1261-1272&rft.issn=1552-4825&rft.eissn=1552-4833&rft_id=info:doi/10.1002/ajmg.a.63142&rft_dat=%3Cproquest_cross%3E2796869654%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2796869654&rft_id=info:pmid/36797513&rfr_iscdi=true |