Literature DB >> 3488053

Congenital stationary night blindness with negative electroretinogram. A new classification.

Y Miyake, K Yagasaki, M Horiguchi, Y Kawase, T Kanda.   

Abstract

An analysis of 64 patients with congenital stationary night blindness showed that all had essentially normal fundi. Electroretinography (ERG) showed a normal a wave with extremely reduced b wave (negative type) when recorded with a single bright white stimulus in the dark. We classified these patients into two groups based on the evaluation of rod ERG and/or psychophysical dark adaptation measured with an 11 degree test target at 15 degrees in the upper part of the retina. One group (35 patients) lacked rod function (complete type). Nine patients could not be classified. No pedigree showed a complete and incomplete type in one family. Differences between the two groups in refractive error, photopic function, and oscillatory potentials in the ERG suggest a different pathogenesis. Our analysis may provide a new classification of congenital stationary night blindness with a negative ERG.

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Year:  1986        PMID: 3488053     DOI: 10.1001/archopht.1986.01050190071042

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


  168 in total

1.  Case of paraneoplastic retinopathy with retinal ON-bipolar cell dysfunction and subsequent resolution of ERGs.

Authors:  Shinji Ueno; Ayami Nakanishi; Kayo Nishi; Shiro Suzuki; Hiroko Terasaki
Journal:  Doc Ophthalmol       Date:  2014-11-13       Impact factor: 2.379

2.  Genotype-phenotype correlation in British families with X linked congenital stationary night blindness.

Authors:  L E Allen; I Zito; K Bradshaw; R J Patel; A C Bird; F Fitzke; J R Yates; D Trump; A J Hardcastle; A T Moore
Journal:  Br J Ophthalmol       Date:  2003-11       Impact factor: 4.638

3.  ERGs in female carriers of incomplete congenital stationary night blindness (I-CSNB). A family report.

Authors:  Florence Rigaudière; Catherine Roux; Pierre Lachapelle; Serge G Rosolen; Pierre Bitoun; Annie Gay-Duval; Jean-François Le Gargasson
Journal:  Doc Ophthalmol       Date:  2003-09       Impact factor: 2.379

4.  An extended 15 Hz ERG protocol (2): data of normal subjects and patients with achromatopsia, CSNB1, and CSNB2.

Authors:  Mieke M C Bijveld; Frans C C Riemslag; Astrid M L Kappers; Frank P Hoeben; Maria M van Genderen
Journal:  Doc Ophthalmol       Date:  2011-09-27       Impact factor: 2.379

5.  Incomplete congenital stationary night blindness: electroretinogram c-wave and electrooculogram light rise.

Authors:  Y Takahashi; S Onoe; N Asamizu; T Mori; Y Yoshimura; Y Tazawa
Journal:  Doc Ophthalmol       Date:  1988-09       Impact factor: 2.379

6.  Spinocerebellar degeneration with negative electroretinogram: dysfunction of the bipolar cells.

Authors:  Akio Kimura; Hideaki Nemoto; Jin Nishimiya; Tatuhiko Yuasa; Hiroko Yamazaki
Journal:  Doc Ophthalmol       Date:  2004-05       Impact factor: 2.379

7.  Is it Usher syndrome? Collaborative diagnosis and molecular genetics of patients with visual impairment and hearing loss.

Authors:  Heather A Stiff; Christina M Sloan-Heggen; Ashley Ko; Wanda L Pfeifer; Diana L Kolbe; Carla J Nishimura; Kathy L Frees; Kevin T Booth; Donghong Wang; Amy E Weaver; Hela Azaiez; John Kamholz; Richard J H Smith; Arlene V Drack
Journal:  Ophthalmic Genet       Date:  2020-04-13       Impact factor: 1.803

8.  Two cases of unilateral cone-rod dysfunction with negative electroretinograms.

Authors:  Kenji Ozawa; Shunsuke Takahashi; Kiyofumi Mochizuki; Yozo Miyake
Journal:  Doc Ophthalmol       Date:  2019-08-02       Impact factor: 2.379

9.  Attenuation of oscillatory potentials in nob2 mice.

Authors:  Minzhong Yu; Neal S Peachey
Journal:  Doc Ophthalmol       Date:  2007-05-04       Impact factor: 2.379

10.  Severe course of cutaneous melanoma associated paraneoplastic retinopathy.

Authors:  U Kellner; N Bornfeld; M H Foerster
Journal:  Br J Ophthalmol       Date:  1995-08       Impact factor: 4.638

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