Literature DB >> 18791549

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

C Gerth1, R J Zawadzki, J S Werner, E Héon.   

Abstract

OBJECTIVES: To investigate retinal microstructure of patients affected with malattia leventinese (MLVT) and mutation in the EFEMP1 gene using high-resolution optical coherence tomography (OCT).
METHODS: Patients diagnosed with MLVT received a comprehensive eye exam, full-field and multifocal electroretinogram testing and imaging with a high-resolution Fourier domain OCT (Fd-OCT, UC Davis Medical Center, Davis, USA; axial resolution: 4.5 microm, acquisition speed: 9 frames s(-1), 1000 A scans s(-1)) combined with a flexible scanning head (Bioptigen Inc. Durham, NC, USA).
RESULTS: Two related patients aged 30 and 60 years, with MLVT and identified c.R345W mutation in the EFEMP1 gene, were tested. Mother and daughter showed a variable phenotype with reduced vision function in the younger patient, whereas the mother had a 'form frustre'. Fd-OCT revealed extensive or focal sub-retinal pigment epithelium (RPE) deposits, separation of RPE and Bruch's membrane, and disruption of the photoreceptor outer and inner segment layers. No outer retinal changes were visible outside areas with sub-RPE deposits.
CONCLUSION: Retinal structure in EFEMP1 retinal dystrophy is reflected by morphological changes within the RPE/Bruch's membrane complex with accumulation of sub-RPE material associated with disrupted photoreceptor integrity. The pattern of microstructural retinal abnormalities is similar but with a different extent in patients with variable phenotypes.

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Year:  2008        PMID: 18791549      PMCID: PMC2734481          DOI: 10.1038/eye.2008.251

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


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Journal:  J Biomed Opt       Date:  2007 Jul-Aug       Impact factor: 3.170

5.  [Hereditary drusen of Bruch's membrane. II: Studies of semi-thin sections and electron microscopy results].

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10.  The R345W mutation in EFEMP1 is pathogenic and causes AMD-like deposits in mice.

Authors:  Li Fu; Donita Garland; Zhenglin Yang; Dhananjay Shukla; Anand Rajendran; Erik Pearson; Edwin M Stone; Kang Zhang; Eric A Pierce
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6.  Retinal imaging in inherited retinal diseases.

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