Literature DB >> 12719092

Foveal thickness in occult macular dystrophy.

Mineo Kondo1, Yasuki Ito, Shinji Ueno, Chang-Hua Piao, Hiroko Terasaki, Yozo Miyake.   

Abstract

PURPOSE: Occult macular dystrophy (OMD) is an inherited macular dystrophy characterized by a progressive macular dysfunction without any visible fundus abnormality. We studied the foveal thickness in patients with OMD using optical coherence tomography (OCT).
DESIGN: Observational case series. Foveal thickness by OCT images.
METHODS: Foveal thickness obtained from 22 eyes of 11 patients with OMD was compared with that from 27 eyes of 20 age-matched normal controls.
RESULTS: Mean foveal thickness in the patients group (96.5 +/- 19.5 microm) was significantly thinner than that in the normal controls (133.3 +/- 9.0 microm, P <.0001, Mann-Whitney U test). Eighteen of 22 eyes with OMD had foveal thickness that were thinner than the lower limit of the normal range. There was no statistically significant correlation between the foveal thickness and visual acuity, age, or duration from onset.
CONCLUSION: These results demonstrated that there are significant anatomic changes in the macula of patients with OMD.

Entities:  

Mesh:

Year:  2003        PMID: 12719092     DOI: 10.1016/s0002-9394(02)02158-x

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


  9 in total

Review 1.  Occult macular dystrophy.

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

2.  Phenotypic characterization of a large family with RP10 autosomal-dominant retinitis pigmentosa: an Asp226Asn mutation in the IMPDH1 gene.

Authors:  Petra Kozma; Dianna K Hughbanks-Wheaton; Kirsten G Locke; Garry E Fish; Anisa I Gire; Catherine J Spellicy; Lori S Sullivan; Sara J Bowne; Stephen P Daiger; David G Birch
Journal:  Am J Ophthalmol       Date:  2005-10-07       Impact factor: 5.258

3.  Ultra-high resolution optical coherence tomography assessment of photoreceptors in retinitis pigmentosa and related diseases.

Authors:  Andre J Witkin; Tony H Ko; James G Fujimoto; Annie Chan; Wolfgang Drexler; Joel S Schuman; Elias Reichel; Jay S Duker
Journal:  Am J Ophthalmol       Date:  2006-09-01       Impact factor: 5.258

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.  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

6.  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

7.  Occult macular dystrophy with bilateral chronic subfoveal serous retinal detachment associated with a novel RP1L1 mutation (p.S1199P).

Authors:  Hidenori Takahashi; Takaaki Hayashi; Hiroshi Tsuneoka; Tadashi Nakano; Hisashi Yamada; Satoshi Katagiri; Yujiro Fujino; Yasuo Noda; Miwako Yoshimoto; Hidetoshi Kawashima
Journal:  Doc Ophthalmol       Date:  2014-05-17       Impact factor: 2.379

8.  Detection of photoreceptor disruption by adaptive optics fundus imaging and Fourier-domain optical coherence tomography in eyes with occult macular dystrophy.

Authors:  Yoshiyuki Kitaguchi; Shunji Kusaka; Tatsuo Yamaguchi; Toshifumi Mihashi; Takashi Fujikado
Journal:  Clin Ophthalmol       Date:  2011-03-10

9.  Structural and functional evaluation of macula in a 9-year-old boy with occult macular dystrophy and his affected elder sibling.

Authors:  Tapas Ranjan Padhi; Chetan Videkar; Subhadra Jalali; Sujoy Mukherjee; Krushna Gopal Panda; Taraprasad Das
Journal:  Oman J Ophthalmol       Date:  2016 Jan-Apr
  9 in total

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