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http://purl.uniprot.org/citations/36797513http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/36797513http://www.w3.org/2000/01/rdf-schema#comment"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."xsd:string
http://purl.uniprot.org/citations/36797513http://purl.org/dc/terms/identifier"doi:10.1002/ajmg.a.63142"xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/author"Grange D.K."xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/author"Palculict T.B."xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/author"Morrow M.M."xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/author"Bupp C."xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/author"Hoover-Fong J.E."xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/author"Beil A."xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/author"Kuentz P."xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/author"Heeley J."xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/author"Delplancq G."xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/author"Pritchard A.B."xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/author"Muss C."xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/author"Albokhari D."xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/author"Zuteck M."xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/date"2023"xsd:gYear
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/name"Am J Med Genet A"xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/pages"1261-1272"xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/title"TELO2-related syndrome (You-Hoover-Fong syndrome): Description of 14 new affected individuals and review of the literature."xsd:string
http://purl.uniprot.org/citations/36797513http://purl.uniprot.org/core/volume"191"xsd:string
http://purl.uniprot.org/citations/36797513http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/36797513
http://purl.uniprot.org/citations/36797513http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/36797513
http://purl.uniprot.org/uniprot/#_B3KMG2-mappedCitation-36797513http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/36797513
http://purl.uniprot.org/uniprot/#_B4DXS2-mappedCitation-36797513http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/36797513