Literature DB >> 18425067

Prevalence of cystic macular lesions in patients with Usher II syndrome.

S Walia1, G A Fishman, M Hajali.   

Abstract

PURPOSE: To evaluate the prevalence of cystic macular lesions in patients with Usher II syndrome.
METHODS: All Usher type II patients seen in the inherited eye disease clinic at the University of Illinois at Chicago between January 2002 and December 2007 were included (n=76). Each participating patient underwent a detailed clinical examination, including best-corrected visual acuity, slit-lamp biomicroscopy and dilated fundus examination. The presence of cystoid lesions was determined by optical coherence tomography (OCT), fundus fluorescein angiogram (FFA), fundus photographs and/or clinical examination.
RESULTS: A cystic-appearing macular change was observed in at least one eye in 19 out of the 76 patients (25%), 13 on the basis of OCT, five using FFA (two solely with the use of FFA and three based on clinical notes and FFA findings) and one based solely on clinical notes. Of the 18 patients with CME, determined by OCT or FFA, five (27.8%) showed either a funduscopically normal-appearing macula (n=4) or an atrophic appearing macular change (n=1).
CONCLUSIONS: One-fourth of our total cohort of Usher II patients had cystic macular lesions. Moreover, a funduscopically normal-appearing macula was observed in 22% (n=4) of our 18 patients with cystic-appearing macular lesions on OCT and/or FFA testing. On the basis of the reasonably high prevalence of cystic macular lesions in our cohort, it would seem prudent to evaluate Usher II patients for the presence of cystoid macular oedema.

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Year:  2008        PMID: 18425067     DOI: 10.1038/eye.2008.105

Source DB:  PubMed          Journal:  Eye (Lond)        ISSN: 0950-222X            Impact factor:   3.775


  9 in total

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2.  Efficacy of sustained topical dorzolamide therapy for cystic macular lesions in patients with retinitis pigmentosa and usher syndrome.

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Authors:  M A Genead; G A Fishman
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Review 4.  [Pharmacological concepts to treat hereditary retinal degenerations].

Authors:  C M Poloschek; H Jägle
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5.  Is it Usher syndrome? Collaborative diagnosis and molecular genetics of patients with visual impairment and hearing loss.

Authors:  Heather A Stiff; Christina M Sloan-Heggen; Ashley Ko; Wanda L Pfeifer; Diana L Kolbe; Carla J Nishimura; Kathy L Frees; Kevin T Booth; Donghong Wang; Amy E Weaver; Hela Azaiez; John Kamholz; Richard J H Smith; Arlene V Drack
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Authors:  Jacque L Duncan; Wendi Liang; Maureen G Maguire; Isabelle Audo; Allison R Ayala; David G Birch; Joseph Carroll; Janet K Cheetham; Simona Degli Esposti; Todd A Durham; Laura Erker; Sina Farsiu; Frederick L Ferris; Elise Heon; Robert B Hufnagel; Alessandro Iannaccone; Glenn J Jaffe; Christine N Kay; Michel Michaelides; Mark E Pennesi; José-Alain Sahel
Journal:  Am J Ophthalmol       Date:  2020-05-22       Impact factor: 5.488

7.  Novel grading system for quantification of cystic macular lesions in Usher syndrome.

Authors:  Ieva Sliesoraityte; Tunde Peto; Saddek Mohand-Said; Jose Alain Sahel
Journal:  Orphanet J Rare Dis       Date:  2015-12-10       Impact factor: 4.123

8.  Retinitis pigmentosa in Usher syndrome in India: Electronic medical records driven big data analytics: Report III.

Authors:  Deepika C Parameswarappa; Anthony Vipin Das; Mariya Bashir Doctor; Ramya Natarajan; Komal Agarwal; Subhadra Jalali
Journal:  Indian J Ophthalmol       Date:  2022-07       Impact factor: 2.969

9.  Werner syndrome with refractory cystoid macular edema and immunohistochemical analysis of WRN proteins in human retinas.

Authors:  Toshiyuki Oshitari; Masayasu Kitahashi; Satoshi Mizuno; Takayuki Baba; Mariko Kubota-Taniai; Minoru Takemoto; Koutaro Yokote; Shuichi Yamamoto; Sayon Roy
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  9 in total

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