Literature DB >> 28197754

Differences in ocular findings in two siblings: one with complete and other with incomplete achromatopsia.

Shinji Ueno1, Ayami Nakanishi2, Akira Sayo2, Taro Kominami2, Yasuki Ito2, Takaaki Hayashi3, Kazushige Tsunoda4, Takeshi Iwata4, Hiroko Terasaki2.   

Abstract

PURPOSE: Patients with complete achromatopsia (ACHM) lack cone function, and patients with incomplete ACHM have relatively good visual acuity with residual color vision. The pathological mechanism(s) underlying incomplete ACHM has not been determined. The purpose of this study was to determine the pathophysiology of ACHM in two siblings: one with complete ACHM and the other with incomplete ACHM.
METHODS: The medical charts of the two siblings were reviewed.
RESULTS: The sibling with incomplete ACHM had decimal visual acuities that ranged from 0.4 to 0.6 and had moderate color blindness in both eyes. Her younger brother was diagnosed with complete ACHM and was not able to hold fixation, had severe pendular nystagmus, visual acuity that ranged from 0.08 to 0.1, and severe color vision abnormalities in both eyes. Optical coherence tomography (OCT) showed that the ellipsoid zone (EZ) was disruptive in the macular region in both patients. However, careful examination of the OCT images in the incomplete ACHM patient showed a high-density EZ in the central fovea. Adaptive optics (AO) fundus imaging of the sibling with incomplete ACHM revealed sparse cone mosaics remaining within 1° of the foveal center with no mosaics visible outside the central fovea. AO fundus imaging could not be performed in Case 2 because of the severe nystagmus.
CONCLUSION: Our results showed that cone mosaics were present in the central fovea in the sibling with incomplete ACHM patient. This may explain the better visual acuity and color vision in this sibling.

Entities:  

Keywords:  Achromatopsia; Adaptive optics (AO) fundus image; Cone mosaic; Incomplete achromatopsia; Optical coherence tomography

Mesh:

Year:  2017        PMID: 28197754     DOI: 10.1007/s10633-017-9577-y

Source DB:  PubMed          Journal:  Doc Ophthalmol        ISSN: 0012-4486            Impact factor:   2.379


  29 in total

1.  Variability in Human Cone Topography Assessed by Adaptive Optics Scanning Laser Ophthalmoscopy.

Authors:  Tianjiao Zhang; Pooja Godara; Ernesto R Blanco; Russell L Griffin; Xiaolin Wang; Christine A Curcio; Yuhua Zhang
Journal:  Am J Ophthalmol       Date:  2015-04-30       Impact factor: 5.258

2.  NEAR-INFRARED REFLECTANCE IMAGING IN EYES WITH ACUTE ZONAL OCCULT OUTER RETINOPATHY.

Authors:  Shinji Ueno; Kenichi Kawano; Yasuki Ito; Eimei Ra; Ayami Nakanishi; Masatoshi Nagaya; Hiroko Terasaki
Journal:  Retina       Date:  2015-08       Impact factor: 4.256

3.  A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene.

Authors:  Bo Chang; Tanja Grau; Susann Dangel; Ron Hurd; Bernhard Jurklies; E Cumhur Sener; Sten Andreasson; Helene Dollfus; Britta Baumann; Sylvia Bolz; Nikolai Artemyev; Susanne Kohl; John Heckenlively; Bernd Wissinger
Journal:  Proc Natl Acad Sci U S A       Date:  2009-11-03       Impact factor: 11.205

4.  Genotype-dependent variability in residual cone structure in achromatopsia: toward developing metrics for assessing cone health.

Authors:  Adam M Dubis; Robert F Cooper; Jonathan Aboshiha; Christopher S Langlo; Venki Sundaram; Benjamin Liu; Frederick Collison; Gerald A Fishman; Anthony T Moore; Andrew R Webster; Alfredo Dubra; Joseph Carroll; Michel Michaelides
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-10-02       Impact factor: 4.799

Review 5.  The cone degenerations.

Authors:  A E Krill; A F Deutman; M Fishman
Journal:  Doc Ophthalmol       Date:  1973-04-16       Impact factor: 2.379

6.  Progressive loss of cones in achromatopsia: an imaging study using spectral-domain optical coherence tomography.

Authors:  Alberta A H J Thiadens; Ville Somervuo; L Ingeborgh van den Born; Susanne Roosing; Mary J van Schooneveld; Robert W A M Kuijpers; Norka van Moll-Ramirez; Frans P M Cremers; Carel B Hoyng; Caroline C W Klaver
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-06-23       Impact factor: 4.799

7.  In vivo imaging of a cone mosaic in a patient with achromatopsia associated with a GNAT2 variant.

Authors:  Shinji Ueno; Ayami Nakanishi; Taro Kominami; Yasuki Ito; Takaaki Hayashi; Kazutoshi Yoshitake; Yuichi Kawamura; Kazushige Tsunoda; Takeshi Iwata; Hiroko Terasaki
Journal:  Jpn J Ophthalmol       Date:  2016-10-07       Impact factor: 2.447

8.  A nonsense mutation in PDE6H causes autosomal-recessive incomplete achromatopsia.

Authors:  Susanne Kohl; Frauke Coppieters; Françoise Meire; Simone Schaich; Susanne Roosing; Christina Brennenstuhl; Sylvia Bolz; Maria M van Genderen; Frans C C Riemslag; Robert Lukowski; Anneke I den Hollander; Frans P M Cremers; Elfride De Baere; Carel B Hoyng; Bernd Wissinger
Journal:  Am J Hum Genet       Date:  2012-08-16       Impact factor: 11.025

9.  Autosomal recessive incomplete achromatopsia with deutan luminosity.

Authors:  V C Smith; J Pokorny; F W Newell
Journal:  Am J Ophthalmol       Date:  1979-03       Impact factor: 5.258

10.  Whole-exome sequencing identifies a novel ALMS1 mutation (p.Q2051X) in two Japanese brothers with Alström syndrome.

Authors:  Satoshi Katagiri; Kazutoshi Yoshitake; Masakazu Akahori; Takaaki Hayashi; Masaaki Furuno; Jo Nishino; Kazuho Ikeo; Hiroshi Tsuneoka; Takeshi Iwata
Journal:  Mol Vis       Date:  2013-11-24       Impact factor: 2.367

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.