Literature DB >> 11786058

Clinical course and visual function in a family with mutations in the RPE65 gene.

Joost Felius1, Debra A Thompson, Naheed W Khan, Eve L Bingham, Jeffrey A Jamison, Jennifer A Kemp, Paul A Sieving.   

Abstract

OBJECTIVE: To evaluate the phenotype of affected and carrier members of a family with mutations in RPE65 (a retinal pigment epithelium gene).
METHODS: RPE65 mutation screening was performed on DNA from 2 affected brothers, 1 unaffected brother, both parents, and 3 surviving grandparents using cycle sequencing. Ophthalmic examinations included ophthalmoscopic fundus examination; visual function testing; 2-color, static, dark-adapted threshold perimetry; and rod electroretinographic a-wave phototransduction analysis.
RESULTS: The 2 affected brothers carried RPE65 mutations in compound heterozygous form: a maternal Y368H (1156T-->C) missense mutation and a paternal IVS1 + 5g-->a splice-site mutation. Severe visual deficits and an absence of rod and cone electroretinographic responses were diagnosed in both affected boys before the age of 5 years. Visual acuities of about 20/100 during grade school declined to hand movements by the teenage years, and only a rudimentary peripheral temporal visual field remained by the ages of 25 and 29 years. Both parents had normal central visual function, as measured by visual acuity, contrast sensitivity, color vision, and Humphrey 10-2 fields. However, the 50-year-old father showed hundreds of tiny whitish hard drusen in both eyes and had abnormal peripheral function on dark-adapted perimetry, with extended field defects of 15 to 20 dB outside 30 degrees eccentricity. His rod photoreceptor sensitivity and amplitude, calculated by fitting the rod a waves by a model of activation of phototransduction, were normal, but the flicker electroretinographic response was delayed.
CONCLUSIONS: The RPE65 mutations Y368H and IVS1 + 5g-->a present in compound heterozygous form cause severe visual compromise in childhood and progress to nearly total vision loss by the second to third decades of life. The retinal and functional changes in the father carrying a presumed functional null allele suggest that some RPE65 heterozygous carriers may manifest visual symptoms.

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Year:  2002        PMID: 11786058     DOI: 10.1001/archopht.120.1.55

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  26 in total

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2.  Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in Denmark.

Authors:  Galuh D N Astuti; Mette Bertelsen; Markus N Preising; Muhammad Ajmal; Birgit Lorenz; Sultana M H Faradz; Raheel Qamar; Rob W J Collin; Thomas Rosenberg; Frans P M Cremers
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3.  Mutation of key residues of RPE65 abolishes its enzymatic role as isomerohydrolase in the visual cycle.

Authors:  T Michael Redmond; Eugenia Poliakov; Shirley Yu; Jen-Yue Tsai; Zhongjian Lu; Susan Gentleman
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4.  Opsin activation of transduction in the rods of dark-reared Rpe65 knockout mice.

Authors:  Jie Fan; Michael L Woodruff; Marianne C Cilluffo; Rosalie K Crouch; Gordon L Fain
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Review 6.  [Genetic diseases of the retinal pigment epithelium].

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9.  Concentric division of 10° visual field tests in retinitis pigmentosa.

Authors:  Ken Ogino; Atsushi Otani; Akio Oishi; Masafumi Kurimoto; Takuro Sekiya; Nagahisa Yoshimura
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10.  Retinoid processing in cone and Müller cell lines.

Authors:  Yogita Kanan; Anne Kasus-Jacobi; Gennadiy Moiseyev; Kjell Sawyer; Jian-Xing Ma; Muayyad R Al-Ubaidi
Journal:  Exp Eye Res       Date:  2007-11-17       Impact factor: 3.467

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