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TELO2-related syndrome (You-Hoover-Fong syndrome): Description of 14 new affected individuals and review of the literature

dc.contributor.authorAlbokhari, Daniah
dc.contributor.authorPritchard, Amanda Barone
dc.contributor.authorBeil, Adelyn
dc.contributor.authorMuss, Candace
dc.contributor.authorBupp, Caleb
dc.contributor.authorGrange, Dorothy K.
dc.contributor.authorDelplancq, Geoffroy
dc.contributor.authorHeeley, Jennifer
dc.contributor.authorZuteck, Melissa
dc.contributor.authorMorrow, Michelle M.
dc.contributor.authorKuentz, Paul
dc.contributor.authorPalculict, Timothy Blake
dc.contributor.authorHoover-Fong, Julie E.
dc.date.accessioned2023-05-01T19:11:38Z
dc.date.available2024-06-01 15:11:36en
dc.date.available2023-05-01T19:11:38Z
dc.date.issued2023-05
dc.identifier.citationAlbokhari, 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. (2023). "TELO2- related syndrome (You- Hoover- Fong syndrome): Description of 14 new affected individuals and review of the literature." American Journal of Medical Genetics Part A 191(5): 1261-1272.
dc.identifier.issn1552-4825
dc.identifier.issn1552-4833
dc.identifier.urihttps://hdl.handle.net/2027.42/176295
dc.description.abstractYou-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.
dc.publisherJohn Wiley & Sons, Inc.
dc.subject.othermicrocephaly
dc.subject.otherdevelopmental delay
dc.subject.otherYou-Hoover-Fong syndrome
dc.subject.otherYHFS
dc.subject.otherTELO2
dc.subject.othersyndromic intellectual disabilities
dc.titleTELO2-related syndrome (You-Hoover-Fong syndrome): Description of 14 new affected individuals and review of the literature
dc.typeArticle
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelHuman Genetics
dc.subject.hlbsecondlevelGenetics
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/176295/1/ajmga63142.pdf
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/176295/2/ajmga63142_am.pdf
dc.identifier.doi10.1002/ajmg.a.63142
dc.identifier.sourceAmerican Journal of Medical Genetics Part A
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dc.working.doiNOen
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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