Literature DB >> 8343466

Cone dystrophies with negative photopic electroretinogram.

U Kellner1, M H Foerster.   

Abstract

A scotopic electroretinogram with an a-wave amplitude larger than the b-wave amplitude traditionally is termed 'negative'. Six male patients with negative photopic electroretinograms were examined; three of them suffered from progressive cone dystrophy, in which negative electroretinograms are unusual. Another patient without symptoms was the brother of a patient with cone dystrophy. These patients are compared with others who characteristically have negative electroretinograms-one patient with incomplete congenital stationary night blindness and another with X linked congenital retinoschisis. Differential diagnosis between these unusual cases of cone dystrophies and X linked retinoschisis or congenital stationary night blindness was possible with funduscopy, adaptometry, and evaluation of progression, but not with the electroretinogram. Inner retinal defects may occur in cone dystrophies as indicated by the negative electroretinogram. The waveform variations between our patients may be due to different inner retinal defects. The findings in two brothers indicate that cone dystrophy and inner retinal defects may be inherited separately.

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Mesh:

Year:  1993        PMID: 8343466      PMCID: PMC504548          DOI: 10.1136/bjo.77.7.404

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  18 in total

1.  CONE DYSFUNCTION SYNDROMES.

Authors:  G GOODMAN; H RIPPS; I M SIEGEL
Journal:  Arch Ophthalmol       Date:  1963-08

2.  Standard for clinical electroretinography. International Standardization Committee.

Authors: 
Journal:  Arch Ophthalmol       Date:  1989-06

3.  Cone-rod dystrophy. Phenotypic diversity by retinal function testing.

Authors:  K Yagasaki; S G Jacobson
Journal:  Arch Ophthalmol       Date:  1989-05

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

Authors:  Y Miyake; K Yagasaki; M Horiguchi; Y Kawase; T Kanda
Journal:  Arch Ophthalmol       Date:  1986-07

5.  Peripheral cone disease.

Authors:  A Pinckers; A F Deutman
Journal:  Ophthalmologica       Date:  1977       Impact factor: 3.250

6.  Selective abnormality of the cone B-wave in a patient with retinal degeneration.

Authors:  R Young; J Price; N Gorham; M Cowart
Journal:  Doc Ophthalmol       Date:  1985-08-30       Impact factor: 2.379

Review 7.  Aland Island eye disease (Forsius-Eriksson syndrome) associated with contiguous deletion syndrome at Xp21. Similarity to incomplete congenital stationary night blindness.

Authors:  R G Weleber; D A Pillers; B R Powell; C E Hanna; R E Magenis; N R Buist
Journal:  Arch Ophthalmol       Date:  1989-08

8.  Bull's eye maculopathy with early cone degeneration.

Authors:  R H Grey; R K Blach; W M Barnard
Journal:  Br J Ophthalmol       Date:  1977-11       Impact factor: 4.638

Review 9.  Blindness from quinine toxicity.

Authors:  P Bacon; D J Spalton; S E Smith
Journal:  Br J Ophthalmol       Date:  1988-03       Impact factor: 4.638

10.  Congenital hereditary (juvenile X-linked) retinoschisis. Histopathologic and ultrastructural findings in three eyes.

Authors:  G P Condon; S Brownstein; N S Wang; J A Kearns; C C Ewing
Journal:  Arch Ophthalmol       Date:  1986-04
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  13 in total

1.  Unilateral electronegative ERG of non-vascular aetiology.

Authors:  A G Robson; E C Richardson; A H C Koh; C E Pavesio; P G Hykin; A Calcagni; E M Graham; G E Holder
Journal:  Br J Ophthalmol       Date:  2005-12       Impact factor: 4.638

2.  Retinal dystrophies with bull's-eye maculopathy along with negative ERGs.

Authors:  F Nasser; A Kurtenbach; S Kohl; C Obermaier; K Stingl; E Zrenner
Journal:  Doc Ophthalmol       Date:  2019-04-03       Impact factor: 2.379

3.  The incidence of negative ERG in clinical practice.

Authors:  A H Koh; C R Hogg; G E Holder
Journal:  Doc Ophthalmol       Date:  2001-01       Impact factor: 2.379

4.  X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.

Authors:  R Jalkanen; M Mäntyjärvi; R Tobias; J Isosomppi; E-M Sankila; T Alitalo; N T Bech-Hansen
Journal:  J Med Genet       Date:  2006-02-27       Impact factor: 6.318

Review 5.  X linked retinoschisis.

Authors:  N D George; J R Yates; A T Moore
Journal:  Br J Ophthalmol       Date:  1995-07       Impact factor: 4.638

6.  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

7.  Electrophysiological evaluation of visual loss in Müller cell sheen dystrophy.

Authors:  U Kellner; H Kraus; H Heimann; H Helbig; N Bornfeld; M H Foerster
Journal:  Br J Ophthalmol       Date:  1998-06       Impact factor: 4.638

8.  Abnormal 8-Hz flicker electroretinograms in carriers of X-linked retinoschisis.

Authors:  J Jason McAnany; Jason C Park; Frederick T Collison; Gerald A Fishman; Edwin M Stone
Journal:  Doc Ophthalmol       Date:  2016-07-01       Impact factor: 2.379

9.  Duchenne muscular dystrophy: negative electroretinograms and normal dark adaptation. Reappraisal of assignment of X linked incomplete congenital stationary night blindness.

Authors:  H Jensen; M Warburg; O Sjö; M Schwartz
Journal:  J Med Genet       Date:  1995-05       Impact factor: 6.318

10.  Autosomal dominant cone-rod dystrophy with negative electroretinogram.

Authors:  N Fujii; T Shiono; Y Wada; M Nakazawa; M Tamai; N Yamada
Journal:  Br J Ophthalmol       Date:  1995-10       Impact factor: 4.638

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