Literature DB >> 12664360

Multifocal electroretinogram (mfERG) in a family with occult macular dystrophy (OMD).

Hannes Wildberger1, Günter Niemeyer, Armin Junghardt.   

Abstract

BACKGROUND: Localized macular dysfunction, in Stargardt macular dystrophy for example, is frequently not detected by Ganzfeld electroretinography (ERG) but it may be detected by methods such as focal macular electroretinogram and pattern electroretinogram at the posterior pole of the eye or indirectly by recording of the visual evoked cortical potentials (VEP). The multifocal electroretinogram (mfERG) is a new diagnostic tool allowing analysis of local bioelectrical signals of circumscript areas across the macular region. Miyake recently described a type of macular dystrophy, which he termed "Occult Macular Dystrophy" (OMD) because of a normal fundus aspect and functional deficit even in aged patients. This is a case report about a family with a presumed OMD where mfERG demonstrated a central depression in the affected family members. PATIENTS AND METHODS: Three members of a family with a suspected autosomal dominant trait complained of a reduced visual acuity since early childhood. The fundus of all patients appeared normal without signs of a maculopathy. The first order mfERG (ROLAND system) was recorded using 61 hexagons.
RESULTS: The signals arising from the macular region of the 6 eyes (3 affected family members) were selectively depressed while the signals from the paracentral area were much less impaired. Statistical analysis of the mfERG signals (concentric hexagon rings) confirmed the central depression with a better performance of the peripheral rings.
CONCLUSIONS: A new family with OMD is added to preceeding reports. A reduced visual acuity without visible fundus abnormalities may be misdiagnosed as amblyopia, optic nerve disease or nonorganic visual disorder. The mfERG offers the diagnostic tool to detect a circumscript retinal/macular dysfunction by a single procedure.

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Mesh:

Year:  2003        PMID: 12664360     DOI: 10.1055/s-2003-38161

Source DB:  PubMed          Journal:  Klin Monbl Augenheilkd        ISSN: 0023-2165            Impact factor:   0.700


  6 in total

Review 1.  Occult macular dystrophy.

Authors:  Yozo Miyake; Kazushige Tsunoda
Journal:  Jpn J Ophthalmol       Date:  2015-02-10       Impact factor: 2.447

2.  Non-familial occult macular dystrophy.

Authors:  Jonathan S Lyons
Journal:  Doc Ophthalmol       Date:  2006-02-25       Impact factor: 2.379

3.  Dominant mutations in RP1L1 are responsible for occult macular dystrophy.

Authors:  Masakazu Akahori; Kazushige Tsunoda; Yozo Miyake; Yoko Fukuda; Hiroyuki Ishiura; Shoji Tsuji; Tomoaki Usui; Tetsuhisa Hatase; Makoto Nakamura; Hisao Ohde; Takeshi Itabashi; Haru Okamoto; Yuichiro Takada; Takeshi Iwata
Journal:  Am J Hum Genet       Date:  2010-09-10       Impact factor: 11.025

4.  Rare occult macular dystrophy with a pathogenic variant in the RP1L1 gene in a patient of Swiss descent.

Authors:  Olga Zabek; Ioannis Lamprakis; Annekatrin Rickmann; Giacomo Calzetti; Bence György; Hendrik P N Scholl; Maria Della Volpe Waizel
Journal:  Am J Ophthalmol Case Rep       Date:  2022-04-10

5.  A 43-year-old man with reduced visual acuity and normal fundus: occult macular dystrophy--case report.

Authors:  Wojciech Lubiński; Wojciech Gosławski; Krzysztof Penkala; Monika Drobek-Słowik; Danuta Karczewicz
Journal:  Doc Ophthalmol       Date:  2007-10-23       Impact factor: 2.379

6.  Utility of en-face imaging in diagnosis of occult macular dystrophy with RP1L1 mutation: A case series.

Authors:  Merry Zc Ruan; S Amal Hussnain; Amanda Thomas; Mahesh Mansukhani; Stephen Tsang; Lawrence Yannuzzi
Journal:  Am J Ophthalmol Case Rep       Date:  2019-05-09
  6 in total

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