Literature DB >> 8721568

The spectrum of ocular features in the Williams-Beuren syndrome.

M Winter1, R Pankau, M Amm, A Gosch, A Wessel.   

Abstract

One hundred and fifty-two patients with the Williams-Beuren syndrome were examined to assess the frequency and severity of ophthalmological features associated with the disorder. Eighty-two (54%) had strabismus, all but three, esotropia. One hundred and seventeen (77%) patients had blue irides, 10 (7%) green, and 25 (16%) brown. One hundred and twelve (74%) showed a typical so-called stellate iris pattern of the anterior stroma. Whitish anomalies were also detectable in brown irides. Two 9-year-old patients and one 46-year-old patient had initial cataract. Of all the patients with funduscopy, 22% had retinal vascular tortuosity. One patient had suspected Rieger syndrome. Two patients had ptosis, one with a Marcus-Gunn phenomenon. No ocular manifestation of hypercalcaemia was noted.

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Year:  1996        PMID: 8721568     DOI: 10.1111/j.1399-0004.1996.tb04320.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  9 in total

Review 1.  Insights into brain development from neurogenetic syndromes: evidence from fragile X syndrome, Williams syndrome, Turner syndrome and velocardiofacial syndrome.

Authors:  E Walter; P K Mazaika; A L Reiss
Journal:  Neuroscience       Date:  2009-04-17       Impact factor: 3.590

Review 2.  Copy number variants at Williams-Beuren syndrome 7q11.23 region.

Authors:  Giuseppe Merla; Nicola Brunetti-Pierri; Lucia Micale; Carmela Fusco
Journal:  Hum Genet       Date:  2010-05-01       Impact factor: 4.132

Review 3.  Conceptualizing neurodevelopmental disorders through a mechanistic understanding of fragile X syndrome and Williams syndrome.

Authors:  Lawrence K Fung; Eve-Marie Quintin; Brian W Haas; Allan L Reiss
Journal:  Curr Opin Neurol       Date:  2012-04       Impact factor: 5.710

4.  Critical buckling pressure in mouse carotid arteries with altered elastic fibers.

Authors:  Callan M Luetkemeyer; Rhys H James; Siva Teja Devarakonda; Victoria P Le; Qin Liu; Hai-Chao Han; Jessica E Wagenseil
Journal:  J Mech Behav Biomed Mater       Date:  2015-02-28

5.  Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevis.

Authors:  Chris Barnett; Oya Yazgan; Hui-Ching Kuo; Sreepurna Malakar; Trevor Thomas; Amanda Fitzgerald; William Harbour; Jonathan J Henry; Jocelyn E Krebs
Journal:  Mech Dev       Date:  2012-06-09       Impact factor: 1.882

6.  Anterior pituitary, sex hormones, and keratoconus: Beyond traditional targets.

Authors:  Dimitrios Karamichos; Paulina Escandon; Brenda Vasini; Sarah E Nicholas; Lyly Van; Deanna H Dang; Rebecca L Cunningham; Kamran M Riaz
Journal:  Prog Retin Eye Res       Date:  2021-11-02       Impact factor: 19.704

7.  Objective differential diagnosis of Noonan and Williams-Beuren syndromes in diverse populations using quantitative facial phenotyping.

Authors:  Antonio R Porras; Marshal Summar; Marius George Linguraru
Journal:  Mol Genet Genomic Med       Date:  2021-03-27       Impact factor: 2.183

Review 8.  Anterior segment dysgenesis associated with Williams-Beuren syndrome: a case report and review of the literature.

Authors:  Margarita G Todorova; Matthias C Grieshaber; Rafael J A Cámara; Peter Miny; Anja M Palmowski-Wolfe
Journal:  BMC Ophthalmol       Date:  2014-05-21       Impact factor: 2.209

9.  Recurrent Rare Copy Number Variants Increase Risk for Esotropia.

Authors:  Mary C Whitman; Silvio Alessandro Di Gioia; Wai-Man Chan; Alon Gelber; Brandon M Pratt; Jessica L Bell; Thomas E Collins; James A Knowles; Christopher Armoskus; Michele Pato; Carlos Pato; Sherin Shaaban; Sandra Staffieri; Sarah MacKinnon; Gail D E Maconachie; James E Elder; Elias I Traboulsi; Irene Gottlob; David A Mackey; David G Hunter; Elizabeth C Engle
Journal:  Invest Ophthalmol Vis Sci       Date:  2020-08-03       Impact factor: 4.799

  9 in total

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