Literature DB >> 9793380

[Hereditary macular dystrophies].

U Kellner1, C Jandeck, H Kraus, M H Foerster.   

Abstract

PURPOSE: Analysis of a consecutive series of patients suffering from hereditary macular dystrophies. PATIENTS AND METHODS: Between 1991 and 1997, 136 patients underwent clinical and electrophysiologic examinations (Ganzfeld ERG, EOG or multifocal ERG).
RESULTS: The time of first examination was similar to the onset of clinical signs in most patients. In half of the patients onset was not before 40 years of age. In younger patients, Stargardt disease, X-linked retinoschisis and Best disease were the most frequent disorders. In patients aged 40 year and older, pattern dystrophies and central areolar choroidal dystrophy were more frequent. In 41 cases (30.2%) a specific diagnosis could not be made. Color vision and multifocal ERG were abnormal in all patients examined. Ganzfeld ERG was important for the diagnosis of X-linked retinoschisis, as was the EOG for Best disease.
CONCLUSIONS: Hereditary macular dystrophies are a heterogeneous group of disorders. In several cases a definite diagnosis could not be made. Pattern dystrophies are the most frequent hereditary macular dystrophies in patients older than 40 years of age.

Entities:  

Mesh:

Year:  1998        PMID: 9793380     DOI: 10.1007/s003470050321

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


  5 in total

1.  [Best's disease with normal EOG. Case report of familial macular dystrophy].

Authors:  K Pollack; F R Kreuz; L E Pillunat
Journal:  Ophthalmologe       Date:  2005-09       Impact factor: 1.059

2.  Detection of retinal dysfunction in vitelliform macular dystrophy using the multifocal ERG (MF-ERG).

Authors:  Anja M Palmowski; Reiner Allgayer; Bernhild Heinemann-Vernaleken; Volker Scherer; Klaus W Ruprecht
Journal:  Doc Ophthalmol       Date:  2003-03       Impact factor: 2.379

Review 3.  Genotype-phenotype correlations and differential diagnosis in autosomal dominant macular disease.

Authors:  A Iannaccone
Journal:  Doc Ophthalmol       Date:  2001-05       Impact factor: 2.379

4.  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

5.  Annular fundus autofluorescence abnormality in a case of macular dystrophy.

Authors:  Charlotte M Poloschek; Lutz L Hansen; Michael Bach
Journal:  Doc Ophthalmol       Date:  2007-11-16       Impact factor: 2.379

  5 in total

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