Literature DB >> 16458713

Optical coherent tomography features of malattia leventinese.

Eric H Souied1, Nicolas Leveziel, Valerie Letien, Jacques Darmon, Gabriel Coscas, Gisele Soubrane.   

Abstract

PURPOSE: Malattia leventinese (ML) is an inherited macular degeneration characterized by the presence of large paracentral and small radial drusen. Our purpose was to describe optical coherent tomography (OCT) features observed in ML.
DESIGN: Prospective observational case series.
METHODS: Ten eyes from five patients with ML aged 27 to 44 years were prospectively included. Best-corrected visual acuity, fundus color photography of the retina, and OCT were performed in each patient.
RESULTS: OCT revealed a hyperreflective thickening of the retinal pigment epithelium-Bruch membrane complex, associated with localized dome-shaped elevations. Retinal thickness above the drusen ranged from 221 to 292 microm (mean 260 microm). Foveal thickness ranged from 72 to 200 microm (mean 144 microm)
CONCLUSIONS: The large paracentral drusen presented either as a thickening of the retinal pigment epithelium-Bruch complex or as local limited elevation of retinal pigment epithelium-Bruch complex, both associated with preservation of the neurosensory retina.

Entities:  

Mesh:

Year:  2006        PMID: 16458713     DOI: 10.1016/j.ajo.2005.09.001

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  8 in total

1.  Analysis of retinal flecks in fundus flavimaculatus using optical coherence tomography.

Authors:  G Querques; N Leveziel; N Benhamou; M Voigt; G Soubrane; E H Souied
Journal:  Br J Ophthalmol       Date:  2006-06-05       Impact factor: 4.638

2.  Retinal microstructure in patients with EFEMP1 retinal dystrophy evaluated by Fourier domain OCT.

Authors:  C Gerth; R J Zawadzki; J S Werner; E Héon
Journal:  Eye (Lond)       Date:  2008-09-12       Impact factor: 3.775

3.  A novel haplotype with the R345W mutation in the EFEMP1 gene associated with autosomal dominant drusen in a Japanese family.

Authors:  Tomokazu Takeuchi; Takaaki Hayashi; Matthew Bedell; Kang Zhang; Hisashi Yamada; Hiroshi Tsuneoka
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-10-22       Impact factor: 4.799

4.  Ultra-High Resolution Optical Coherence Tomography Imaging of Unilateral Drusen in a 31 Year Old Woman.

Authors:  Talisa E de Carlo; Mehreen Adhi; Chen D Lu; Jay S Duker; James G Fujimoto; Nadia K Waheed
Journal:  Clin Med Rev Case Rep       Date:  2015-10-10

Review 5.  Macular dystrophies: clinical and imaging features, molecular genetics and therapeutic options.

Authors:  Najiha Rahman; Michalis Georgiou; Kamron N Khan; Michel Michaelides
Journal:  Br J Ophthalmol       Date:  2019-11-08       Impact factor: 4.638

6.  Quantifying the Separation Between the Retinal Pigment Epithelium and Bruch's Membrane using Optical Coherence Tomography in Patients with Inherited Macular Degeneration.

Authors:  Kamron N Khan; Shyamanga Borooah; Leonardo Lando; Kunny Dans; Omar A Mahroo; Amit Meshi; Angelos Kalitzeos; Georgios Agorogiannis; Sasan Moghimi; William R Freeman; Andrew R Webster; Anthony T Moore; Martin McKibbin; Michel Michaelides
Journal:  Transl Vis Sci Technol       Date:  2020-05-23       Impact factor: 3.283

7.  Retinal imaging in inherited retinal diseases.

Authors:  Michalis Georgiou; Kaoru Fujinami; Michel Michaelides
Journal:  Ann Eye Sci       Date:  2020-09-15

8.  Diagnostic definition of malattia leventinese in a family from Colombia

Authors:  Nancy Gelvez; Paula Hurtado-Villa; Silvia Flórez; Anne Charlotte Brieke; Francisco Rodríguez; Ana María Bertolotto; Martha L Tamayo
Journal:  Biomedica       Date:  2021-09-22       Impact factor: 0.935

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.