Literature DB >> 19190919

[Clinical findings and diagnostics of cone dystrophy].

U Kellner1, S Kellner.   

Abstract

BACKGROUND: Cone dystrophies present with highly variable clinical findings and often limited retinal changes, which may lead to misdiagnosis. The purpose of the present review of the clinical presentation and diagnosis of cone dystrophies is to provide guidelines for improved patient care.
METHODS: A literature search and evaluation of the clinical findings were carried out in 450 patients with cone dystrophy examined between 1986 and 2008.
RESULTS: Characteristic signs are loss of visual acuity, photophobia and central scotoma. The diagnosis of cone dystrophy is determined by a full-field electroretinogram (ERG). Fundus and near-infrared autofluorescence as well as optical coherence tomography allow detection of retinal structural abnormalities even when findings from ophthalmoscopy are normal.
CONCLUSION: The diagnosis of cone dystrophy is difficult due to unspecific subjective symptoms and absence of characteristic ophthalmoscopic findings. The differential diagnosis of unexplained visual loss should include cone dystrophy and requires either a full-field or multifocal ERG.

Entities:  

Mesh:

Year:  2009        PMID: 19190919     DOI: 10.1007/s00347-008-1863-3

Source DB:  PubMed          Journal:  Ophthalmologe        ISSN: 0941-293X            Impact factor:   1.059


  29 in total

1.  Cone and rod function in cone degenerations.

Authors:  B Sadowski; E Zrenner
Journal:  Vision Res       Date:  1997-08       Impact factor: 1.886

2.  Quantitative analysis of OCT characteristics in patients with achromatopsia and blue-cone monochromatism.

Authors:  Daniel Barthelmes; Florian K Sutter; Malaika M Kurz-Levin; Martina M Bosch; Horst Helbig; Günter Niemeyer; Johannes C Fleischhauer
Journal:  Invest Ophthalmol Vis Sci       Date:  2006-03       Impact factor: 4.799

3.  Blue cone monochromatism: clinical findings in patients with mutations in the red/green opsin gene cluster.

Authors:  Ulrich Kellner; Bernd Wissinger; Sabine Tippmann; Susanne Kohl; Hannelore Kraus; Michael H Foerster
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2004-09       Impact factor: 3.117

4.  Peripheral cone dystrophy: a variant of cone dystrophy with predominant dysfunction in the peripheral cone system.

Authors:  Mineo Kondo; Yozo Miyake; Nagako Kondo; Shinji Ueno; Hideo Takakuwa; Hiroko Terasaki
Journal:  Ophthalmology       Date:  2004-04       Impact factor: 12.079

5.  Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.

Authors:  Bernd Wissinger; Susann Dangel; Herbert Jägle; Lars Hansen; Britta Baumann; Günther Rudolph; Christiane Wolf; Michael Bonin; Katja Koeppen; Thomas Ladewig; Susanne Kohl; Eberhart Zrenner; Thomas Rosenberg
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-02       Impact factor: 4.799

6.  Cone dystrophies with negative photopic electroretinogram.

Authors:  U Kellner; M H Foerster
Journal:  Br J Ophthalmol       Date:  1993-07       Impact factor: 4.638

7.  Abnormal cone synapses in human cone-rod dystrophy.

Authors:  K Gregory-Evans; R N Fariss; D E Possin; C Y Gregory-Evans; A H Milam
Journal:  Ophthalmology       Date:  1998-12       Impact factor: 12.079

8.  A pilot study of Fourier-domain optical coherence tomography of retinal dystrophy patients.

Authors:  Jennifer I Lim; Ou Tan; Amani A Fawzi; J Jill Hopkins; John H Gil-Flamer; David Huang
Journal:  Am J Ophthalmol       Date:  2008-07-17       Impact factor: 5.258

Review 9.  Cone rod dystrophies.

Authors:  Christian P Hamel
Journal:  Orphanet J Rare Dis       Date:  2007-02-01       Impact factor: 4.123

Review 10.  Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update.

Authors:  Anthony G Robson; Michel Michaelides; Zubin Saihan; Alan C Bird; Andrew R Webster; Anthony T Moore; Fred W Fitzke; Graham E Holder
Journal:  Doc Ophthalmol       Date:  2007-11-06       Impact factor: 2.379

View more
  5 in total

1.  [Cone dystrophy--of the significance of a minority of photoreceptors].

Authors:  B Wissinger
Journal:  Ophthalmologe       Date:  2009-02       Impact factor: 1.059

2.  Multimodal imaging of foveal cavitation in retinal dystrophies.

Authors:  Maurizio Battaglia Parodi; Maria Vittoria Cicinelli; Pierluigi Iacono; Gianluigi Bolognesi; Francesco Bandello
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2016-08-05       Impact factor: 3.117

3.  [Morphological characteristics in macular telangiectasia type 2].

Authors:  P Charbel Issa; T F C Heeren; E Krüger; M Zeimer; D Pauleikhoff; F G Holz
Journal:  Ophthalmologe       Date:  2014-09       Impact factor: 1.059

Review 4.  Macular telangiectasia type 2.

Authors:  Peter Charbel Issa; Mark C Gillies; Emily Y Chew; Alan C Bird; Tjebo F C Heeren; Tunde Peto; Frank G Holz; Hendrik P N Scholl
Journal:  Prog Retin Eye Res       Date:  2012-12-03       Impact factor: 21.198

5.  A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defect.

Authors:  Susanne Kohl; Pablo Llavona; Alexandra Sauer; Peggy Reuter; Nicole Weisschuh; Melanie Kempf; Florian Alexander Dehmelt; Aristides B Arrenberg; Ieva Sliesoraityte; Eberhart Zrenner; Mary J van Schooneveld; Günther Rudolph; Laura Kühlewein; Bernd Wissinger
Journal:  Hum Mol Genet       Date:  2021-06-17       Impact factor: 6.150

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.