Literature DB >> 21473666

Anterior segment abnormalities and angle-closure glaucoma in a family with a mutation in the BEST1 gene and Best vitelliform macular dystrophy.

Elisabeth Wittström1, Vesna Ponjavic, Marie-Louise Bondeson, Sten Andréasson.   

Abstract

PURPOSE: To present the clinical and electrophysiological findings in four members of a family with Best vitelliform macular dystrophy (BVMD) and angle-closure glaucoma (ACG).
METHODS: Four members of a family with BVMD were examined clinically, including visual acuity, slit-lamp examination, biomicroscopy, Goldmann applanation tonometry and gonioscopy. Measurements of the anterior chamber depth and axial length, visual field, optical coherence tomography, full-field electroretinography, multifocal electroretinography and electrooculography were performed. In addition molecular genetic analysis of the bestrophin-1 gene (BEST1), the microphthalmia-associated transcription factor gene (MITF) and the cone-rod homeobox gene (CRX) were performed.
RESULTS: Four family members with the c.253T>C p.Y85H mutation in the BEST1 gene and BVMD in different stages also exhibited anterior segment abnormalities such as shallow anterior chambers (two cases), and reduced axial lengths in all cases. Microphthalmos (axial length ≤ 20mm) was found in the index patient and in her son. Hyperopia was found in all four examined patients. Closed angles/narrow angles were observed in patients with microphthalmos. The index patient developed ACG at the age of 12 years. Her son inherited microphthalmos, severe hyperopia, and narrow angles. He is at risk of developing ACG. No pathogenic mutation of the MITF or the CRX genes was detected in the index patient.
CONCLUSIONS: BVMD could be associated with anterior segment abnormalities such as shallow anterior chambers, closed/narrow anterior chamber angles and ACG. Ophthalmologists should be aware of the association between ACG and BVMD. Examination of the anterior segment, gonioscopy and intraocular pressure control are recommended in patients with BVMD.

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Year:  2011        PMID: 21473666     DOI: 10.3109/13816810.2011.567884

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN: 1381-6810            Impact factor:   1.803


  12 in total

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2.  Structure and insights into the function of a Ca(2+)-activated Cl(-) channel.

Authors:  Veronica Kane Dickson; Leanne Pedi; Stephen B Long
Journal:  Nature       Date:  2014-10-22       Impact factor: 49.962

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Authors:  Mohammed Ziaei; Ashkan Khalili; Richard Wormald
Journal:  Int Ophthalmol       Date:  2013-04-08       Impact factor: 2.031

4.  Quantitative fundus autofluorescence and optical coherence tomography in best vitelliform macular dystrophy.

Authors:  Tobias Duncker; Jonathan P Greenberg; Rithambara Ramachandran; Donald C Hood; R Theodore Smith; Tatsuo Hirose; Russell L Woods; Stephen H Tsang; François C Delori; Janet R Sparrow
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-03-13       Impact factor: 4.799

5.  Autosomal dominant Best disease with an unusual electrooculographic light rise and risk of angle-closure glaucoma: a clinical and molecular genetic study.

Authors:  Sancy Low; Alice E Davidson; Graham E Holder; Chris R Hogg; Shomi S Bhattacharya; Graeme C Black; Paul J Foster; Andrew R Webster
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6.  Autosomal recessive bestrophinopathy associated with angle-closure glaucoma.

Authors:  C Crowley; R Paterson; T Lamey; T McLaren; J De Roach; E Chelva; J Khan
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7.  Bestrophin 1 gene analysis and associated clinical findings in a Chinese patient with Best vitelliform macular dystrophy.

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Journal:  Mol Med Rep       Date:  2017-08-04       Impact factor: 2.952

8.  Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series.

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Journal:  PLoS One       Date:  2017-01-05       Impact factor: 3.240

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Journal:  Mol Med Rep       Date:  2018-05-23       Impact factor: 2.952

10.  Genetic variations in Bestrophin‑1 and associated clinical findings in two Chinese patients with juvenile‑onset and adult‑onset best vitelliform macular dystrophy.

Authors:  Ying Lin; Tao Li; Chenghong Ma; Hongbin Gao; Chuan Chen; Yi Zhu; Bingqian Liu; Yu Lian; Ying Huang; Haichun Li; Qingxiu Wu; Xiaoling Liang; Chenjin Jin; Xinhua Huang; Jianhua Ye; Lin Lu
Journal:  Mol Med Rep       Date:  2017-10-27       Impact factor: 2.952

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