Literature DB >> 17525851

[Genetic and clinical heterogeneity in LCA patients. The end of uniformity].

M N Preising1, K Paunescu, C Friedburg, B Lorenz.   

Abstract

BACKGROUND: Leber congenital amaurosis (LCA) usually describes patients with severely reduced vision due to a retinal dystrophy in early childhood.
METHODS: In 135 families in a case series with severely reduced vision due to a retinal dystrophy in early childhood a complete ophthalmologic examination was extended by two-color threshold perimetry, fundus autofluorescence (FAF), und optical coherence tomography (OCT). Mutation screening included AIPL1, CRB1, CRX, GUCY2D, LRAT, RPE65, RPGRIP, and TULP1.
RESULTS: GUCY2D mutations caused the most severe phenotype with severely reduced vision from birth but unremarkable fundus appearance. RPE65 mutations were correlated with an obvious lack of FAF. CRB1 mutations showed a significantly thickened retina on OCT. CRX mutations were associated with a progressive form of cone-rod dystrophy.
CONCLUSION: A genotype-phenotype correlation for selected genes allows an optimized strategy for the molecular genetic work-up.

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Year:  2007        PMID: 17525851     DOI: 10.1007/s00347-007-1533-x

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


  42 in total

1.  Null RPGRIP1 alleles in patients with Leber congenital amaurosis.

Authors:  T P Dryja; S M Adams; J L Grimsby; T L McGee; D H Hong; T Li; S Andréasson; E L Berson
Journal:  Am J Hum Genet       Date:  2001-03-29       Impact factor: 11.025

2.  Early-onset severe rod-cone dystrophy in young children with RPE65 mutations.

Authors:  B Lorenz; P Gyürüs; M Preising; D Bremser; S Gu; M Andrassi; C Gerth; A Gal
Journal:  Invest Ophthalmol Vis Sci       Date:  2000-08       Impact factor: 4.799

3.  Study of the involvement of the RGR, CRPB1, and CRB1 genes in the pathogenesis of autosomal recessive retinitis pigmentosa.

Authors:  S Bernal; M Calaf; M Garcia-Hoyos; B Garcia-Sandoval; J Rosell; A Adan; C Ayuso; M Baiget
Journal:  J Med Genet       Date:  2003-07       Impact factor: 6.318

4.  Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome.

Authors:  Enza Maria Valente; Jennifer L Silhavy; Francesco Brancati; Giuseppe Barrano; Suguna Rani Krishnaswami; Marco Castori; Madeline A Lancaster; Eugen Boltshauser; Loredana Boccone; Lihadh Al-Gazali; Elisa Fazzi; Sabrina Signorini; Carrie M Louie; Emanuele Bellacchio; Enrico Bertini; Bruno Dallapiccola; Joseph G Gleeson
Journal:  Nat Genet       Date:  2006-05-07       Impact factor: 38.330

5.  Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination.

Authors:  Samuel G Jacobson; Artur V Cideciyan; Tomas S Aleman; Michael J Pianta; Alexander Sumaroka; Sharon B Schwartz; Elaine E Smilko; Ann H Milam; Val C Sheffield; Edwin M Stone
Journal:  Hum Mol Genet       Date:  2003-05-01       Impact factor: 6.150

Review 6.  Genotype-phenotype correlation in a German family with a novel complex CRX mutation extending the open reading frame.

Authors:  K Paunescu; M N Preising; B Janke; B Wissinger; B Lorenz
Journal:  Ophthalmology       Date:  2007-02-22       Impact factor: 12.079

7.  Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle.

Authors:  Debra A Thompson; Andreas R Janecke; Jessica Lange; Kecia L Feathers; Christian A Hübner; Christina L McHenry; David W Stockton; Gabriele Rammesmayer; James R Lupski; Guillermo Antinolo; Carmen Ayuso; Montserrat Baiget; Peter Gouras; John R Heckenlively; Anneke den Hollander; Samuel G Jacobson; Richard A Lewis; Paul A Sieving; Bernd Wissinger; Suzanne Yzer; Eberhart Zrenner; Gerd Utermann; Andreas Gal
Journal:  Hum Mol Genet       Date:  2005-11-03       Impact factor: 6.150

8.  Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis.

Authors:  H Morimura; G A Fishman; S A Grover; A B Fulton; E L Berson; T P Dryja
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-17       Impact factor: 11.205

9.  Identification of a locus (LCA9) for Leber's congenital amaurosis on chromosome 1p36.

Authors:  T Jeffrey Keen; Moin D Mohamed; Martin McKibbin; Yasmin Rashid; Hussain Jafri; Irene H Maumenee; Chris F Inglehearn
Journal:  Eur J Hum Genet       Date:  2003-05       Impact factor: 4.246

10.  Evidence of a founder effect for the RETGC1 (GUCY2D) 2943DelG mutation in Leber congenital amaurosis pedigrees of Finnish origin.

Authors:  Sylvain Hanein; Isabelle Perrault; Päivi Olsen; Tuija Lopponen; Marja Hietala; Sylvie Gerber; Marc Jeanpierre; Fabienne Barbet; Dominique Ducroq; Sélim Hakiki; Arnold Munnich; Jean-Michel Rozet; Josseline Kaplan
Journal:  Hum Mutat       Date:  2002-10       Impact factor: 4.878

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  7 in total

1.  Mutations in RD3 are associated with an extremely rare and severe form of early onset retinal dystrophy.

Authors:  Markus N Preising; Nora Hausotter-Will; Manuel C Solbach; Christoph Friedburg; Franz Rüschendorf; Birgit Lorenz
Journal:  Invest Ophthalmol Vis Sci       Date:  2012-06-08       Impact factor: 4.799

Review 2.  [Genetic diseases of the retinal pigment epithelium].

Authors:  M N Preising; B Lorenz
Journal:  Ophthalmologe       Date:  2009-04       Impact factor: 1.059

3.  Impact of LCA-Associated E14L LRAT Mutation on Protein Stability and Retinoid Homeostasis.

Authors:  Sylwia Chelstowska; Made Airanthi K Widjaja-Adhi; Josie A Silvaroli; Marcin Golczak
Journal:  Biochemistry       Date:  2017-08-15       Impact factor: 3.162

Review 4.  Role of carotenoids and retinoids during heart development.

Authors:  Ioan Ovidiu Sirbu; Aimée Rodica Chiş; Alexander Radu Moise
Journal:  Biochim Biophys Acta Mol Cell Biol Lipids       Date:  2020-01-22       Impact factor: 4.698

Review 5.  Lecithin:Retinol Acyltransferase: A Key Enzyme Involved in the Retinoid (visual) Cycle.

Authors:  Avery E Sears; Krzysztof Palczewski
Journal:  Biochemistry       Date:  2016-05-23       Impact factor: 3.162

Review 6.  Molecular Basis for Vitamin A Uptake and Storage in Vertebrates.

Authors:  Sylwia Chelstowska; Made Airanthi K Widjaja-Adhi; Josie A Silvaroli; Marcin Golczak
Journal:  Nutrients       Date:  2016-10-26       Impact factor: 5.717

7.  Long-Term Follow-Up of Retinal Degenerations Associated With LRAT Mutations and Their Comparability to Phenotypes Associated With RPE65 Mutations.

Authors:  Mays Talib; Mary J van Schooneveld; Roos J G van Duuren; Caroline Van Cauwenbergh; Jacoline B Ten Brink; Elfride De Baere; Ralph J Florijn; Nicoline E Schalij-Delfos; Bart P Leroy; Arthur A Bergen; Camiel J F Boon
Journal:  Transl Vis Sci Technol       Date:  2019-08-19       Impact factor: 3.283

  7 in total

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