Literature DB >> 25940553

Retinal structure in young patients aged 10 years or less with Best vitelliform macular dystrophy.

Patrik Schatz1,2,3, Dror Sharon4, Sermed Al-Hamdani5,6, Sten Andréasson7, Michael Larsen5,6,8.   

Abstract

PURPOSE: Our aim was to analyze retinal structure in young patients with Best disease with reference to future gene therapy.
METHODS: This was a retrospective observational spectral domain optical coherence tomography study of four patients aged 10 years or less with Best disease.
RESULTS: Findings ranged from subtle thickening at the level of the retinal pigment epithelium-photoreceptor interdigitation line, to subretinal fluid and precipitate-like changes at the level of the photoreceptor outer segments, and further to choroidal neovascularization. The photoreceptor inner segment ellipsoid layer could be visualized seemingly undisturbed above the vitelliform lesions, except in the case of choroidal neovascularization.
CONCLUSIONS: Clinical variability is evident even among young patients aged 10 years or less with Best disease. The earliest structural alterations seem to occur at the level of the retinal pigment epithelium-photoreceptor interdigitation line. The photoreceptor inner segment seems to be unaffected unless choroidal neovascularization develops, which seems promising regarding future gene therapy.

Entities:  

Keywords:  BEST1; Best vitelliform macular dystrophy; Optical coherence tomography; Retinal degeneration

Mesh:

Substances:

Year:  2015        PMID: 25940553     DOI: 10.1007/s00417-015-3025-z

Source DB:  PubMed          Journal:  Graefes Arch Clin Exp Ophthalmol        ISSN: 0721-832X            Impact factor:   3.117


  22 in total

1.  Visual outcome following subretinal hemorrhage in Best disease.

Authors:  M M Chung; K T Oh; L M Streb; A E Kimura; E M Stone
Journal:  Retina       Date:  2001       Impact factor: 4.256

2.  Identification of the gene responsible for Best macular dystrophy.

Authors:  K Petrukhin; M J Koisti; B Bakall; W Li; G Xie; T Marknell; O Sandgren; K Forsman; G Holmgren; S Andreasson; M Vujic; A A Bergen; V McGarty-Dugan; D Figueroa; C P Austin; M L Metzker; C T Caskey; C Wadelius
Journal:  Nat Genet       Date:  1998-07       Impact factor: 38.330

3.  Role of bestrophin-1 in store-operated calcium entry in retinal pigment epithelium.

Authors:  Néstor Más Gómez; Ernst R Tamm; Olaf Strauβ
Journal:  Pflugers Arch       Date:  2012-12-04       Impact factor: 3.657

4.  Autosomal recessive best vitelliform macular dystrophy: report of a family and management of early-onset neovascular complications.

Authors:  Alessandro Iannaccone; Natalie C Kerr; Tyson R Kinnick; Jorge I Calzada; Edwin M Stone
Journal:  Arch Ophthalmol       Date:  2011-02

5.  The spectrum of subclinical Best vitelliform macular dystrophy in subjects with mutations in BEST1 gene.

Authors:  Giuseppe Querques; Jennyfer Zerbib; Rossana Santacroce; Maurizio Margaglione; Nathalie Delphin; Lea Querques; Jean-Michel Rozet; Josseline Kaplan; Eric H Souied
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-06-28       Impact factor: 4.799

6.  Frequency and clinical pattern of vitelliform macular dystrophy caused by mutations of interphotoreceptor matrix IMPG1 and IMPG2 genes.

Authors:  Isabelle Meunier; Gaël Manes; Béatrice Bocquet; Virginie Marquette; Corinne Baudoin; Bernard Puech; Sabine Defoort-Dhellemmes; Isabelle Audo; Robert Verdet; Carl Arndt; Xavier Zanlonghi; Guylène Le Meur; Claire-Marie Dhaenens; Christian P Hamel
Journal:  Ophthalmology       Date:  2014-07-29       Impact factor: 12.079

7.  ADVIRC is caused by distinct mutations in BEST1 that alter pre-mRNA splicing.

Authors:  R Burgess; R E MacLaren; A E Davidson; J E Urquhart; G E Holder; A G Robson; A T Moore; R O' Keefe; G C M Black; F D C Manson
Journal:  J Med Genet       Date:  2008-07-08       Impact factor: 6.318

8.  Biallelic mutation of BEST1 causes a distinct retinopathy in humans.

Authors:  Rosemary Burgess; Ian D Millar; Bart P Leroy; Jill E Urquhart; Ian M Fearon; Elfrida De Baere; Peter D Brown; Anthony G Robson; Genevieve A Wright; Philippe Kestelyn; Graham E Holder; Andrew R Webster; Forbes D C Manson; Graeme C M Black
Journal:  Am J Hum Genet       Date:  2008-01       Impact factor: 11.025

9.  Mutations in IMPG1 cause vitelliform macular dystrophies.

Authors:  Gaël Manes; Isabelle Meunier; Almudena Avila-Fernández; Sandro Banfi; Guylène Le Meur; Xavier Zanlonghi; Marta Corton; Francesca Simonelli; Philippe Brabet; Gilles Labesse; Isabelle Audo; Saddek Mohand-Said; Christina Zeitz; José-Alain Sahel; Michel Weber; Hélène Dollfus; Claire-Marie Dhaenens; Delphine Allorge; Elfride De Baere; Robert K Koenekoop; Susanne Kohl; Frans P M Cremers; Joe G Hollyfield; Audrey Sénéchal; Maxime Hebrard; Béatrice Bocquet; Carmen Ayuso García; Christian P Hamel
Journal:  Am J Hum Genet       Date:  2013-08-29       Impact factor: 11.025

10.  Clinical evaluation of two consanguineous families with homozygous mutations in BEST1.

Authors:  Teresa Piñeiro-Gallego; María Álvarez; Inés Pereiro; Severiano Campos; Dror Sharon; Patrik Schatz; Diana Valverde
Journal:  Mol Vis       Date:  2011-06-16       Impact factor: 2.367

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  2 in total

1.  Impaired Bestrophin Channel Activity in an iPSC-RPE Model of Best Vitelliform Macular Dystrophy (BVMD) from an Early Onset Patient Carrying the P77S Dominant Mutation.

Authors:  Arnau Navinés-Ferrer; Sheila Ruiz-Nogales; Rafael Navarro; Esther Pomares
Journal:  Int J Mol Sci       Date:  2022-07-04       Impact factor: 6.208

2.  Multimodal Image Analysis in Acquired Vitelliform Lesions and Adult-Onset Foveomacular Vitelliform Dystrophy.

Authors:  Ricardo Rocha Bastos; Carla Sofia Ferreira; Elisete Brandão; Fernando Falcão-Reis; Ângela M Carneiro
Journal:  J Ophthalmol       Date:  2016-04-12       Impact factor: 1.909

  2 in total

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