Literature DB >> 22139616

Unilateral retinitis pigmentosa: a proposal of genetic pathogenic mechanisms.

Marcela Marsiglia1, Tobias Duncker, Enrico Peiretti, Scott E Brodie, Stephen H Tsang.   

Abstract

PURPOSE: To investigate and integrate anatomic and physiologic findings from a group of patients who present retinitis pigmentosa affecting just one eye and use this information to propose mechanisms of disease pathogenesis.
METHODS: This prospective cross-sectional study examined 5 patients, all female, from 8 to 60 years old. The study was conducted in 4 university hospitals. The patients were selected according to the characteristics of ocular involvement, notably unilateral presentation of similar anatomic and functional abnormalities. Full-field electroretinogram, fundus photography, fundus autofluorescence, infrared imaging, optical coherence tomography, and genetic testing were performed.
RESULTS: Full-field electroretinogram showed unilateral decrease in amplitude and increase in implicit time; autofluorescence showed unilateral areas of decreased intensity. The USH2AW4149R mutation was confirmed in one patient.
CONCLUSIONS: Imaging and functional testing are important in elucidating the unilateral pattern of the disease and in monitoring these individuals. Mosaicism or somatic mutation may cause unilateral genetic disease presentation.

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Year:  2012        PMID: 22139616      PMCID: PMC3705904          DOI: 10.5301/ejo.5000086

Source DB:  PubMed          Journal:  Eur J Ophthalmol        ISSN: 1120-6721            Impact factor:   2.597


  26 in total

1.  Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa.

Authors:  Terri L McGee; Babak Jian Seyedahmadi; Meredith O Sweeney; Thaddeus P Dryja; Eliot L Berson
Journal:  J Med Genet       Date:  2010-05-27       Impact factor: 6.318

2.  Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity.

Authors:  A G Robson; Z Saihan; S A Jenkins; F W Fitzke; A C Bird; A R Webster; G E Holder
Journal:  Br J Ophthalmol       Date:  2006-04       Impact factor: 4.638

3.  Unilateral retinitis pigmentosa; report of a case.

Authors:  D M GORDON
Journal:  Am J Ophthalmol       Date:  1949-10       Impact factor: 5.258

4.  Unilateral retinitis pigmentosa occurring in an individual with a germline mutation in the RP1 gene.

Authors:  Rajarshi Mukhopadhyay; Graham E Holder; Anthony T Moore; Andrew R Webster
Journal:  Arch Ophthalmol       Date:  2011-07

5.  Identification of disease-causing mutations in autosomal dominant retinitis pigmentosa (adRP) using next-generation DNA sequencing.

Authors:  Sara J Bowne; Lori S Sullivan; Daniel C Koboldt; Li Ding; Robert Fulton; Rachel M Abbott; Erica J Sodergren; David G Birch; Dianna H Wheaton; John R Heckenlively; Qin Liu; Eric A Pierce; George M Weinstock; Stephen P Daiger
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-01-25       Impact factor: 4.799

6.  Bilateral disc edema and unilateral macular hole in a patient with retinitis pigmentosa.

Authors:  S Ozdek; S Ozdogan; T Sezgin; G Gurelik
Journal:  Eur J Ophthalmol       Date:  2006 May-Jun       Impact factor: 2.597

7.  [Unilateral pigmented paravenous retinochoroidal atrophy].

Authors:  P Charbel Issa; H P Scholl; H-M Helb; M Fleckenstein; C Inhetvin-Hutter; F G Holz
Journal:  Klin Monbl Augenheilkd       Date:  2007-10       Impact factor: 0.700

8.  Blood-retinal barrier breakdown in retinitis pigmentosa: light and electron microscopic immunolocalization.

Authors:  S A Vinores; M Küchle; N L Derevjanik; J D Henderer; J Mahlow; W R Green; P A Campochiaro
Journal:  Histol Histopathol       Date:  1995-10       Impact factor: 2.303

9.  Mutation analysis of 272 Spanish families affected by autosomal recessive retinitis pigmentosa using a genotyping microarray.

Authors:  Almudena Ávila-Fernández; Diego Cantalapiedra; Elena Aller; Elena Vallespín; Jana Aguirre-Lambán; Fiona Blanco-Kelly; M Corton; Rosa Riveiro-Álvarez; Rando Allikmets; María José Trujillo-Tiebas; José M Millán; Frans P M Cremers; Carmen Ayuso
Journal:  Mol Vis       Date:  2010-12-03       Impact factor: 2.367

Review 10.  Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update.

Authors:  Anthony G Robson; Michel Michaelides; Zubin Saihan; Alan C Bird; Andrew R Webster; Anthony T Moore; Fred W Fitzke; Graham E Holder
Journal:  Doc Ophthalmol       Date:  2007-11-06       Impact factor: 2.379

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  9 in total

1.  Multimodal Imaging of Central Retinal Disease Progression in a 2-Year Mean Follow-up of Retinitis Pigmentosa.

Authors:  Tharikarn Sujirakul; Michael K Lin; Jimmy Duong; Ying Wei; Sara Lopez-Pintado; Stephen H Tsang
Journal:  Am J Ophthalmol       Date:  2015-07-09       Impact factor: 5.258

2.  Two cases of unilateral cone-rod dysfunction presenting in adult females.

Authors:  Stephanie Choi; Saagar A Pandit; Archana A Nair; Vivienne Greenstein; Steven L Galetta; Scott E Brodie
Journal:  Doc Ophthalmol       Date:  2022-09-07       Impact factor: 1.854

3.  Unilateral retinitis pigmentosa occurring in an individual with a mutation in the CLRN1 gene.

Authors:  Peng Yong Sim; V Swetha E Jeganathan; Alan F Wright; Peter Cackett
Journal:  BMJ Case Rep       Date:  2018-03-15

4.  Unilateral retinitis pigmentosa: 30 years follow-up.

Authors:  Julia M Weller; Georg Michelson; Anselm G Juenemann
Journal:  BMJ Case Rep       Date:  2014-02-10

5.  Witnessing the first sign of retinitis pigmentosa onset in the allegedly normal eye of a case of unilateral RP: a 30-year follow-up.

Authors:  Mathieu Gauvin; Hadi Chakor; Robert K Koenekoop; John M Little; Jean-Marc Lina; Pierre Lachapelle
Journal:  Doc Ophthalmol       Date:  2016-04-04       Impact factor: 2.379

6.  Concurrent retinitis pigmentosa and pigmented paravenous retinochoroidal atrophy phenotypes in the same patient.

Authors:  Dhanashree Ratra; Dhileesh P Chandrasekharan; P Aruldas; Vineet Ratra
Journal:  Indian J Ophthalmol       Date:  2016-10       Impact factor: 1.848

7.  Unilateral Retinitis Pigmentosa Associated with Possible Ciliopathy and a Novel Mutation.

Authors:  Doaa Milibari; Moustafa Magliyah; Valmore A Semidey; Patrik Schatz; Hani B ALBalawi
Journal:  Clin Pract       Date:  2022-07-05

8.  Characterization of macular structure and function in two Swedish families with genetically identified autosomal dominant retinitis pigmentosa.

Authors:  Wissam Abdulridha-Aboud; Ulrika Kjellström; Sten Andréasson; Vesna Ponjavic
Journal:  Mol Vis       Date:  2016-05-22       Impact factor: 2.367

Review 9.  Unilateral pigmentary retinopathy--a review of literature and case presentation.

Authors:  Alina-Cristina Stamate; Marian Burcea; Mihail Zemba
Journal:  Rom J Ophthalmol       Date:  2016 Jan-Mar
  9 in total

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