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Article: Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome

TitleExpanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome
Authors
Keywordshypertrichosis
KMT2A
MLL1
syndromic intellectual disability
syndromic short stature
Issue Date2021
PublisherJohn Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jabout/33129/ProductInformation.html
Citation
American Journal of Medical Genetics Part A, 2021, v. 185 n. 6, p. 1649-1665 How to Cite?
AbstractWiedemann-Steiner syndrome (WSS) is an autosomal dominant disorder caused by monoallelic variants in KMT2A and characterized by intellectual disability and hypertrichosis. We performed a retrospective, multicenter, observational study of 104 individuals with WSS from five continents to characterize the clinical and molecular spectrum of WSS in diverse populations, to identify physical features that may be more prevalent in White versus Black Indigenous People of Color individuals, to delineate genotype–phenotype correlations, to define developmental milestones, to describe the syndrome through adulthood, and to examine clinicians' differential diagnoses. Sixty-nine of the 82 variants (84%) observed in the study were not previously reported in the literature. Common clinical features identified in the cohort included: developmental delay or intellectual disability (97%), constipation (63.8%), failure to thrive (67.7%), feeding difficulties (66.3%), hypertrichosis cubiti (57%), short stature (57.8%), and vertebral anomalies (46.9%). The median ages at walking and first words were 20 months and 18 months, respectively. Hypotonia was associated with loss of function (LoF) variants, and seizures were associated with non-LoF variants. This study identifies genotype–phenotype correlations as well as race-facial feature associations in an ethnically diverse cohort, and accurately defines developmental trajectories, medical comorbidities, and long-term outcomes in individuals with WSS.
Persistent Identifierhttp://hdl.handle.net/10722/298670
ISSN
2023 Impact Factor: 1.7
2023 SCImago Journal Rankings: 0.718
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorSheppard, SE-
dc.contributor.authorCampbell, IM-
dc.contributor.authorHarr, MH-
dc.contributor.authorGold, N-
dc.contributor.authorLi, D-
dc.contributor.authorBjomsoon, HT-
dc.contributor.authorCohen, JS-
dc.contributor.authorFahrner, JA-
dc.contributor.authorFatemi, A-
dc.contributor.authorHarris, JR-
dc.contributor.authorNowak, C-
dc.contributor.authorZadeh, N-
dc.contributor.authorZand, DJ-
dc.contributor.authorFalk, MJ-
dc.contributor.authorHakonarson, H-
dc.contributor.authorZackai, EH-
dc.contributor.authorQuintero-Rivera, F-
dc.contributor.authorStevens, CA-
dc.contributor.authorGrand, K-
dc.contributor.authorAu, M-
dc.contributor.authorGraham, JM-
dc.contributor.authorSanchez-Lara, PA-
dc.contributor.authorCampo, MD-
dc.contributor.authorJones, MC-
dc.contributor.authorAbdul-Rahman, O-
dc.contributor.authorAlkuraya, FS-
dc.contributor.authorBassetti, JA-
dc.contributor.authorBergstrom, K-
dc.contributor.authorBhoj, E-
dc.contributor.authorDugan, S-
dc.contributor.authorKaplan, JD-
dc.contributor.authorDerar, N-
dc.contributor.authorGripp, KW-
dc.contributor.authorHauser, N-
dc.contributor.authorInnes, AM-
dc.contributor.authorKeena, B-
dc.contributor.authorKodra, N-
dc.contributor.authorMiller, R-
dc.contributor.authorNelson, B-
dc.contributor.authorNowaczyk, MJ-
dc.contributor.authorRahbeeni, Z-
dc.contributor.authorBen-Shachar, S-
dc.contributor.authorShieh, JT-
dc.contributor.authorSlavotinek, A-
dc.contributor.authorSobering, AK-
dc.contributor.authorAbbott, MA-
dc.contributor.authorAllain, DC-
dc.contributor.authorAmlie-Wolf, L-
dc.contributor.authorAu, PYB-
dc.contributor.authorBedoukian, E-
dc.contributor.authorBeek, G-
dc.contributor.authorBarry, J-
dc.contributor.authorBerg, J-
dc.contributor.authorBernstein, JA-
dc.contributor.authorCytrynbaum, C-
dc.contributor.authorChung, BHY-
dc.contributor.authorDonoghue, S-
dc.contributor.authorDorrani, N-
dc.contributor.authorEaton, A-
dc.contributor.authorFlores-Daboub, JA-
dc.contributor.authorDubbs, H-
dc.contributor.authorFelix, CA-
dc.contributor.authorFong, CT-
dc.contributor.authorFung, LF-
dc.contributor.authorGangaram, B-
dc.contributor.authorGoldstein, A-
dc.contributor.authorGreenberg, R-
dc.contributor.authorHa, TK-
dc.contributor.authorHersh, J-
dc.contributor.authorIzumi, K-
dc.contributor.authorKallish, S-
dc.contributor.authorKravets, E-
dc.contributor.authorKwok, PY-
dc.contributor.authorJobling, RK-
dc.contributor.authorKnight Johnson, AE-
dc.contributor.authorKushner, J-
dc.contributor.authorLee, BH-
dc.contributor.authorLevin, B-
dc.contributor.authorLindstrom, K-
dc.contributor.authorManickam, K-
dc.contributor.authorMardach, R-
dc.contributor.authorMcCormick, E-
dc.contributor.authorMcLeod, DR-
dc.contributor.authorMentch, FD-
dc.contributor.authorMinks, K-
dc.contributor.authorMuraresku, C-
dc.contributor.authorNelson, SF-
dc.contributor.authorPorazzi, P-
dc.contributor.authorPichurin, PN-
dc.contributor.authorPowell-Hamilton, NN-
dc.contributor.authorPowis, Z-
dc.contributor.authorRitter, A-
dc.contributor.authorRogers, C-
dc.contributor.authorRohena, L-
dc.contributor.authorRonspies, C-
dc.contributor.authorSchroeder, A-
dc.contributor.authorStark, Z-
dc.contributor.authorStarr, L-
dc.contributor.authorStoler, J-
dc.contributor.authorSuwannarat, P-
dc.contributor.authorVelinov, M-
dc.contributor.authorWeksberg, R-
dc.contributor.authorWilnai, Y-
dc.date.accessioned2021-04-12T03:01:44Z-
dc.date.available2021-04-12T03:01:44Z-
dc.date.issued2021-
dc.identifier.citationAmerican Journal of Medical Genetics Part A, 2021, v. 185 n. 6, p. 1649-1665-
dc.identifier.issn1552-4825-
dc.identifier.urihttp://hdl.handle.net/10722/298670-
dc.description.abstractWiedemann-Steiner syndrome (WSS) is an autosomal dominant disorder caused by monoallelic variants in KMT2A and characterized by intellectual disability and hypertrichosis. We performed a retrospective, multicenter, observational study of 104 individuals with WSS from five continents to characterize the clinical and molecular spectrum of WSS in diverse populations, to identify physical features that may be more prevalent in White versus Black Indigenous People of Color individuals, to delineate genotype–phenotype correlations, to define developmental milestones, to describe the syndrome through adulthood, and to examine clinicians' differential diagnoses. Sixty-nine of the 82 variants (84%) observed in the study were not previously reported in the literature. Common clinical features identified in the cohort included: developmental delay or intellectual disability (97%), constipation (63.8%), failure to thrive (67.7%), feeding difficulties (66.3%), hypertrichosis cubiti (57%), short stature (57.8%), and vertebral anomalies (46.9%). The median ages at walking and first words were 20 months and 18 months, respectively. Hypotonia was associated with loss of function (LoF) variants, and seizures were associated with non-LoF variants. This study identifies genotype–phenotype correlations as well as race-facial feature associations in an ethnically diverse cohort, and accurately defines developmental trajectories, medical comorbidities, and long-term outcomes in individuals with WSS.-
dc.languageeng-
dc.publisherJohn Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jabout/33129/ProductInformation.html-
dc.relation.ispartofAmerican Journal of Medical Genetics Part A-
dc.rightsSubmitted (preprint) Version This is the pre-peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. Accepted (peer-reviewed) Version This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.-
dc.subjecthypertrichosis-
dc.subjectKMT2A-
dc.subjectMLL1-
dc.subjectsyndromic intellectual disability-
dc.subjectsyndromic short stature-
dc.titleExpanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome-
dc.typeArticle-
dc.identifier.emailChung, BHY: bhychung@hku.hk-
dc.identifier.emailFung, LF: jasflfs@HKUCC-COM.hku.hk-
dc.identifier.authorityChung, BHY=rp00473-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/ajmg.a.62124-
dc.identifier.pmid33783954-
dc.identifier.scopuseid_2-s2.0-85103413428-
dc.identifier.hkuros322137-
dc.identifier.volume185-
dc.identifier.issue6-
dc.identifier.spage1649-
dc.identifier.epage1665-
dc.identifier.isiWOS:000634871800001-
dc.publisher.placeUnited States-

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