Literature DB >> 14991316

[Clinical and genetic findings in a patient with fundus albipunctatus].

K Rüther1, B P M Janssen, U Kellner, J J M Janssen, M Bohne, J Reimann, C A G G Driessen.   

Abstract

METHODS: The 38-year-old index patient was examined by visual acuity testing, perimetry, dark adaptometry, funduscopy, electroretinogram (ERG), and multifocal ERG. She was screened for mutations in exons 2-5 and exon/intron boundaries of the 11- cis retinol dehydrogenase gene by direct sequencing.
RESULTS: Visual acuity was 1.0, but perimetry revealed paracentral scotomas associated with reading problems. The optic discs were normal. After 45 min of darkness there was nearly no increase of light sensitivity. After 30 min of dark adaptation, the scotopic ERG showed reduced amplitudes, but after 60 min a nearly normal level was reached. The 30-Hz flicker response of the cone ERG showed borderline implicit times, but no reduction of amplitudes. However, multifocal ERG clearly disclosed a paracentral amplitude reduction as the reason for the visual field defects. The fundus was typical for fundus albipunctatus. The patient is a compound heterozygote carrying a Ile33Asn and a Arg157Trp mutation.
CONCLUSIONS: The paracentral visual field defects were due to cone dysfunction. So far the patient exhibits no cone dystrophy.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 14991316     DOI: 10.1007/s00347-003-0895-y

Source DB:  PubMed          Journal:  Ophthalmologe        ISSN: 0941-293X            Impact factor:   1.059


  18 in total

1.  A frequent 1085delC/insGAAG mutation in the RDH5 gene in Japanese patients with fundus albipunctatus.

Authors:  Y Wada; T Abe; N Fuse; M Tamai
Journal:  Invest Ophthalmol Vis Sci       Date:  2000-06       Impact factor: 4.799

Review 2.  Confronting complexity: the interlink of phototransduction and retinoid metabolism in the vertebrate retina.

Authors:  J K McBee; K Palczewski; W Baehr; D R Pepperberg
Journal:  Prog Retin Eye Res       Date:  2001-07       Impact factor: 21.198

3.  Disruption of the 11-cis-retinol dehydrogenase gene leads to accumulation of cis-retinols and cis-retinyl esters.

Authors:  C A Driessen; H J Winkens; K Hoffmann; L D Kuhlmann; B P Janssen; A H Van Vugt; J P Van Hooser; B E Wieringa; A F Deutman; K Palczewski; K Ruether; J J Janssen
Journal:  Mol Cell Biol       Date:  2000-06       Impact factor: 4.272

4.  Rod and cone visual cycle consequences of a null mutation in the 11-cis-retinol dehydrogenase gene in man.

Authors:  Artur V Cideciyan; Françoise Haeseleer; Robert N Fariss; Tomas S Aleman; Geeng-Fu Jang; Christophe L M J Verlinde; Michael F Marmor; Samuel G Jacobson; Krzysztof Palczewski
Journal:  Vis Neurosci       Date:  2000 Sep-Oct       Impact factor: 3.241

5.  11-cis retinol dehydrogenase mutations as a major cause of the congenital night-blindness disorder known as fundus albipunctatus.

Authors:  F Gonzalez-Fernandez; D Kurz; Y Bao; S Newman; B P Conway; J E Young; D P Han; S C Khani
Journal:  Mol Vis       Date:  1999-12-30       Impact factor: 2.367

6.  Null mutation in the human 11-cis retinol dehydrogenase gene associated with fundus albipunctatus.

Authors:  C A Driessen; B P Janssen; H J Winkens; L D Kuhlmann; A H Van Vugt; A J Pinckers; A F Deutman; J J Janssen
Journal:  Ophthalmology       Date:  2001-08       Impact factor: 12.079

7.  The retinal pigment epithelial-specific 11-cis retinol dehydrogenase belongs to the family of short chain alcohol dehydrogenases.

Authors:  A Simon; U Hellman; C Wernstedt; U Eriksson
Journal:  J Biol Chem       Date:  1995-01-20       Impact factor: 5.157

8.  Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus.

Authors:  H Yamamoto; A Simon; U Eriksson; E Harris; E L Berson; T P Dryja
Journal:  Nat Genet       Date:  1999-06       Impact factor: 38.330

9.  Cloning and expression of a cDNA encoding bovine retinal pigment epithelial 11-cis retinol dehydrogenase.

Authors:  C A Driessen; B P Janssen; H J Winkens; A H van Vugt; T L de Leeuw; J J Janssen
Journal:  Invest Ophthalmol Vis Sci       Date:  1995-09       Impact factor: 4.799

View more
  7 in total

1.  [Classification of biomedical research reports as a reference for evidence-based medicine in ophthalmology. A survey considering as example the journal Der Ophthalmologe].

Authors:  H P N Scholl; M Fleckenstein; T U Krohne; F G Holz
Journal:  Ophthalmologe       Date:  2005-12       Impact factor: 1.059

2.  A large animal model of RDH5-associated retinopathy recapitulates important features of the human phenotype.

Authors:  Laurence M Occelli; Anahita Daruwalla; Samantha R De Silva; Paige A Winkler; Kelian Sun; Nathaniel Pasmanter; Andrea Minella; Janice Querubin; Leslie A Lyons; Anthony G Robson; Elise Heon; Michel Michaelides; Andrew R Webster; Krzysztof Palczewski; Ajoy Vincent; Omar A Mahroo; Philip D Kiser; Simon M Petersen-Jones
Journal:  Hum Mol Genet       Date:  2022-04-22       Impact factor: 5.121

3.  Fundus albipunctatus: novel mutations and phenotypic description of Israeli patients.

Authors:  Eran Pras; Elon Pras; Haike Reznik-Wolf; Dror Sharon; Svetlana Raivech; Yaniv Barkana; Almogit Abu-Horowitz; Rotenstreich Ygal; Eyal Banin
Journal:  Mol Vis       Date:  2012-06-23       Impact factor: 2.367

4.  Novel mutations in RDH5 cause fundus albipunctatus in two consanguineous Pakistani families.

Authors:  Muhammad Ajmal; Muhammad Imran Khan; Kornelia Neveling; Yar Muhammad Khan; Syeda Hafiza Benish Ali; Waqas Ahmed; Muhammad Safdar Iqbal; Maleeha Azam; Anneke I den Hollander; Rob W J Collin; Raheel Qamar; Frans P M Cremers
Journal:  Mol Vis       Date:  2012-06-13       Impact factor: 2.367

Review 5.  Fundus albipunctatus: review of the literature and report of a novel RDH5 gene mutation affecting the invariant tyrosine (p.Tyr175Phe).

Authors:  Anna Skorczyk-Werner; Przemysław Pawłowski; Marta Michalczuk; Alicja Warowicka; Anna Wawrocka; Katarzyna Wicher; Alina Bakunowicz-Łazarczyk; Maciej R Krawczyński
Journal:  J Appl Genet       Date:  2015-03-28       Impact factor: 3.240

6.  Novel variants in the RDH5 Gene in a Chinese Han family with fundus albipunctatus.

Authors:  Tianwei Qian; Qiaoyun Gong; Hangqi Shen; Caihua Li; Gao Wang; Xun Xu; Isabelle Schrauwen; Weijun Wang
Journal:  BMC Ophthalmol       Date:  2022-02-11       Impact factor: 2.209

7.  A Novel Pathogenic Variant in the RDH5 Gene in a Patient with Fundus Albipunctatus and Severe Macular Atrophy.

Authors:  Hyelin You; David Sierpina
Journal:  Case Rep Genet       Date:  2022-04-06
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.