Literature DB >> 8312830

Clinical findings in patients with congenital stationary night blindness of the Schubert-Bornschein type.

K Ruether1, E Apfelstedt-Sylla, E Zrenner.   

Abstract

We examined 23 patients (18 families) with congenital stationary night blindness (CSNB) who showed a "negative" electroretinogram of the Schubert-Bornschein type. The goal of the study was to find evidence for the classification proposed by Miyake (complete and incomplete type) based on electroretinograms (ERGs) and dark-adaptation function and to look for additional classification parameters that argue for or against heterogeneity. In all, 13 patients revealed the complete type and 10 the incomplete type. The mean age of our patients was 24.7 years (median, 21 years; SD, 14.5 years). In both groups, almost all patients were myopic (mean, -6.05 D; SD, 3.77 D; median, -6.12 D), and there was a reduction in visual acuity (mean, 0.34; SD, 0.14; median, 0.35) without significant differences between the subgroups. In all, 56.5% of the patients suffered from nystagmus and 52.2% squinted. These results confirm the Miyake classification and suggest that only ERG and dark-adaptation data allow a discrimination between the two subtypes. The ongoing molecular analysis will show whether there are correlates on the molecular level.

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Year:  1993        PMID: 8312830

Source DB:  PubMed          Journal:  Ger J Ophthalmol        ISSN: 0941-2921


  7 in total

1.  [Multimodal diagnostic of CSNB1 with NYX gene mutation].

Authors:  P Rating; H Stöhr; C Neuhaus; B Schaperdoth-Gerlings; M R R Böhm; M-A Freimuth; N E Bechrakis
Journal:  Ophthalmologe       Date:  2019-12       Impact factor: 1.059

2.  Isolation and characterization of the leucine-rich proteoglycan nyctalopin gene (cNyx) from chick.

Authors:  N Torben Bech-Hansen; Josh Cockfield; Dan Liu; C Cairine Logan
Journal:  Mamm Genome       Date:  2005-10-29       Impact factor: 2.957

3.  TRPM1 mutations are associated with the complete form of congenital stationary night blindness.

Authors:  Makoto Nakamura; Rikako Sanuki; Tetsuhiro R Yasuma; Akishi Onishi; Koji M Nishiguchi; Chieko Koike; Mikiko Kadowaki; Mineo Kondo; Yozo Miyake; Takahisa Furukawa
Journal:  Mol Vis       Date:  2010-03-12       Impact factor: 2.367

4.  A patient diagnosed with Galloway-Mowat syndrome presenting with a rod-cone functional anomaly with electronegative dark-adapted ERGs.

Authors:  Julie Racine; Richard Golden
Journal:  Doc Ophthalmol       Date:  2021-02-06       Impact factor: 2.379

5.  A novel large in-frame deletion within the CACNA1F gene associates with a cone-rod dystrophy 3-like phenotype.

Authors:  Jan Hauke; Andrea Schild; Antje Neugebauer; Alexandra Lappa; Julia Fricke; Sascha Fauser; Stefanie Rösler; Andrea Pannes; Dirk Zarrinnam; Janine Altmüller; Susanne Motameny; Gudrun Nürnberg; Peter Nürnberg; Eric Hahnen; Bodo B Beck
Journal:  PLoS One       Date:  2013-10-04       Impact factor: 3.240

6.  Targeting ON-bipolar cells by AAV gene therapy stably reverses LRIT3-congenital stationary night blindness.

Authors:  Keiko Miyadera; Evelyn Santana; Karolina Roszak; Sommer Iffrig; Meike Visel; Simone Iwabe; Ryan F Boyd; Joshua T Bartoe; Yu Sato; Alexa Gray; Ana Ripolles-Garcia; Valérie L Dufour; Leah C Byrne; John G Flannery; William A Beltran; Gustavo D Aguirre
Journal:  Proc Natl Acad Sci U S A       Date:  2022-03-22       Impact factor: 12.779

7.  Assessment of age changes and repeatability for computer-based rod dark adaptation.

Authors:  Laura Patryas; Neil R A Parry; David Carden; Daniel H Baker; Jeremiah M F Kelly; Tariq Aslam; Ian J Murray
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2013-04-05       Impact factor: 3.117

  7 in total

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