Literature DB >> 8587019

Electrophysiological and eye-movement abnormalities in children with the Bardet-Biedl syndrome.

T Lavy1, C M Harris, F Shawkat, D Thompson, D Taylor, A Kriss.   

Abstract

We investigated 17 patients with clinical features of Bardet-Biedl syndrome by electroretinogram (ERG), visual-evoked potentials (VEP), and electro-oculographic (EOG) eye movement assessment. The ERGs were grossly abnormal in 16 cases. Pattern VEPs were generally well preserved, but showed a tendency to increase in latency and decrease in amplitude with age. These results confirm other reports that the retinopathy appears to be a progressive rod-cone dystrophy initially affecting mainly extramacular areas but involving the macula at later stages. Seven of 11 patients showed abnormalities of either optokinetic nystagmus, vestibulo-ocular reflex, or both. These eye-movement abnormalities have not been reported previously, and are further evidence of central nervous system involvement in this syndrome.

Entities:  

Mesh:

Year:  1995        PMID: 8587019     DOI: 10.3928/0191-3913-19951101-08

Source DB:  PubMed          Journal:  J Pediatr Ophthalmol Strabismus        ISSN: 0191-3913            Impact factor:   1.402


  5 in total

1.  Intrafamilial variation of the phenotype in Bardet-Biedl syndrome.

Authors:  R Riise; S Andréasson; M K Borgaström; A F Wright; N Tommerup; T Rosenberg; K Tornqvist
Journal:  Br J Ophthalmol       Date:  1997-05       Impact factor: 4.638

2.  Evolution of ocular clinical and electrophysiological findings in pediatric Bardet-Biedl syndrome.

Authors:  E Spaggiari; R Salati; P Nicolini; R Borgatti; U Pozzoli; F Polenghi
Journal:  Int Ophthalmol       Date:  1999       Impact factor: 2.031

3.  ERGs, cone-isolating VEPs and analytical techniques in children with cone dysfunction syndromes.

Authors:  John P Kelly; Michael A Crognale; Avery H Weiss
Journal:  Doc Ophthalmol       Date:  2003-05       Impact factor: 2.379

4.  Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity.

Authors:  Erica R Eichers; Muhammad M Abd-El-Barr; Richard Paylor; Richard Alan Lewis; Weimin Bi; Xiaodi Lin; Thomas P Meehan; David W Stockton; Samuel M Wu; Elizabeth Lindsay; Monica J Justice; Philip L Beales; Nicholas Katsanis; James R Lupski
Journal:  Hum Genet       Date:  2006-06-23       Impact factor: 4.132

5.  Ophthalmic and Genetic Features of Bardet Biedl Syndrome in a German Cohort.

Authors:  Fadi Nasser; Susanne Kohl; Anne Kurtenbach; Melanie Kempf; Saskia Biskup; Theresia Zuleger; Tobias B Haack; Nicole Weisschuh; Katarina Stingl; Eberhart Zrenner
Journal:  Genes (Basel)       Date:  2022-07-08       Impact factor: 4.141

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.