Literature DB >> 2774037

Hereditary macular dystrophy without visible fundus abnormality.

Y Miyake1, K Ichikawa, Y Shiose, Y Kawase.   

Abstract

We found an unusual form of macular dystrophy in three patients from two generations of the same family. The fundi of these patients appeared normal by ophthalmoscopy and fluorescein angiography, even in an older patient and in patients with poor visual acuity. Results of full-field electroretinograms were also normal in both cone and rod components. Focal macular electroretinograms were severely affected, however, indicating retinal impairment in the macular region. Results of Tübingen perimetry were consistent with electroretinographic findings. Since the condition was progressive, this disease is thought to be a hereditary macular dystrophy without visible fundus abnormality.

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Year:  1989        PMID: 2774037     DOI: 10.1016/0002-9394(89)90120-7

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  28 in total

1.  Evaluation of the LKC stimulator for focal ERG testing.

Authors:  J S Lyons; D J Sapper
Journal:  Doc Ophthalmol       Date:  2001-09       Impact factor: 2.379

2.  Occult macular dystrophy in an 11 year old boy.

Authors:  M Kondo; S Ueno; C-H Piao; Y Ito; H Terasaki; Y Miyake
Journal:  Br J Ophthalmol       Date:  2004-12       Impact factor: 4.638

Review 3.  Occult macular dystrophy.

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

4.  Detection of ophthalmoscopically occult maculopathy by focal electroretinography.

Authors:  E T Schmeisser; A D Epstein
Journal:  Doc Ophthalmol       Date:  2001-11       Impact factor: 2.379

5.  Non-familial occult macular dystrophy.

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

6.  Characterizing the phenotype and genotype of a family with occult macular dystrophy.

Authors:  Connie J Chen; Hendrik P N Scholl; David G Birch; Takeshi Iwata; Neil R Miller; Morton F Goldberg
Journal:  Arch Ophthalmol       Date:  2012-12

7.  Elderly case of pseudo-unilateral occult macular dystrophy with Arg45Trp mutation in RP1L1 gene.

Authors:  Takashi Okuno; Takaaki Hayashi; Jun Sugasawa; Hidehiro Oku; Hisashi Yamada; Hiroshi Tsuneoka; Tsunehiko Ikeda
Journal:  Doc Ophthalmol       Date:  2013-04-26       Impact factor: 2.379

8.  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

9.  Pattern-reversal visual-evoked potential in patients with occult macular dystrophy.

Authors:  Gen Hanazono; Hisao Ohde; Kei Shinoda; Kazushige Tsunoda; Kazuo Tsubota; Yozo Miyake
Journal:  Clin Ophthalmol       Date:  2010-12-10

10.  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

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