Literature DB >> 12642313

Progression of phenotype in Leber's congenital amaurosis with a mutation at the LCA5 locus.

M D Mohamed1, N C Topping, H Jafri, Y Raashed, M A McKibbin, C F Inglehearn.   

Abstract

BACKGROUND: Leber's congenital amaurosis (LCA) accounts for 5% of inherited retinal disease and is usually inherited as an autosomal recessive trait. Genetic and clinical heterogeneity exist. Mutations have been described in the RPE65, CRB1, RPGRIP1, AIPL1, GUCY2D, and CRX genes and other pedigrees show linkage to the LCA3 and LCA5 loci. The latter is a new locus which maps to 6q11-q16. The ocular findings and the evolution of the macula staphyloma are described in five members of a Pakistani family with consanguinity and a mutation in the LCA5 gene.
METHODS: 13 family members including five affected individuals consented to DNA analysis and ocular examination including fundal photography.
RESULTS: Ocular abnormalities are described. The most striking feature was the progression of macula abnormalities in three brothers resulting in a colobomatous appearance in the eldest compared to only mild atrophy in the youngest. The phenotypic pattern of this mutation in this Pakistani family contrasts with the "Old Order River Brethren" who were of Swiss descent, in whom the mutation was first described.
CONCLUSION: The evolution of a new phenotypic picture is presented to a mutation in LCA5.

Entities:  

Mesh:

Year:  2003        PMID: 12642313      PMCID: PMC1771622          DOI: 10.1136/bjo.87.4.473

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  15 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.  Clinical spectrum of leber's congenital amaurosis in the second to fourth decades of life.

Authors:  D Smith; J Oestreicher; M A Musarella
Journal:  Ophthalmology       Date:  1990-09       Impact factor: 12.079

3.  ON VARIOUS RECESSIVE BIOTYPES OF LEBER'S CONGENITAL AMAUROSIS.

Authors:  P J WAARDENBURG; J SCHAPPERT-KIMMIJSER
Journal:  Acta Ophthalmol (Copenh)       Date:  1963

4.  The natural history of Leber's congenital amaurosis. Age-related findings in 35 patients.

Authors:  K L Heher; E I Traboulsi; I H Maumenee
Journal:  Ophthalmology       Date:  1992-02       Impact factor: 12.079

Review 5.  Mechanisms of cell death in the inherited retinal degenerations.

Authors:  G H Travis
Journal:  Am J Hum Genet       Date:  1998-03       Impact factor: 11.025

6.  Mutations in the CRB1 gene cause Leber congenital amaurosis.

Authors:  A J Lotery; S G Jacobson; G A Fishman; R G Weleber; A B Fulton; P Namperumalsamy; E Héon; A V Levin; S Grover; J R Rosenow; K K Kopp; V C Sheffield; E M Stone
Journal:  Arch Ophthalmol       Date:  2001-03

7.  Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis.

Authors:  M M Sohocki; S J Bowne; L S Sullivan; S Blackshaw; C L Cepko; A M Payne; S S Bhattacharya; S Khaliq; S Qasim Mehdi; D G Birch; W R Harrison; F F Elder; J R Heckenlively; S P Daiger
Journal:  Nat Genet       Date:  2000-01       Impact factor: 38.330

8.  Concordance and recessive inheritance of Leber congenital amaurosis.

Authors:  S R Lambert; S Sherman; D Taylor; A Kriss; R Coffey; M Pembrey
Journal:  Am J Med Genet       Date:  1993-05-15

9.  Retinal-specific guanylate cyclase gene mutations in Leber's congenital amaurosis.

Authors:  I Perrault; J M Rozet; P Calvas; S Gerber; A Camuzat; H Dollfus; S Châtelin; E Souied; I Ghazi; C Leowski; M Bonnemaison; D Le Paslier; J Frézal; J L Dufier; S Pittler; A Munnich; J Kaplan
Journal:  Nat Genet       Date:  1996-12       Impact factor: 38.330

10.  Mutation analysis of 3 genes in patients with Leber congenital amaurosis.

Authors:  A J Lotery; P Namperumalsamy; S G Jacobson; R G Weleber; G A Fishman; M A Musarella; C S Hoyt; E Héon; A Levin; J Jan; B Lam; R E Carr; A Franklin; S Radha; J L Andorf; V C Sheffield; E M Stone
Journal:  Arch Ophthalmol       Date:  2000-04
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  11 in total

1.  Longitudinal clinical course of three Japanese patients with Leber congenital amaurosis/early-onset retinal dystrophy with RDH12 mutation.

Authors:  Kazuki Kuniyoshi; Hiroyuki Sakuramoto; Kazutoshi Yoshitake; Kosuke Abe; Kazuho Ikeo; Masaaki Furuno; Kazushige Tsunoda; Shunji Kusaka; Yoshikazu Shimomura; Takeshi Iwata
Journal:  Doc Ophthalmol       Date:  2014-04-22       Impact factor: 2.379

Review 2.  Leber congenital amaurosis, from darkness to light: An ode to Irene Maumenee.

Authors:  Razek Georges Coussa; Irma Lopez Solache; Robert K Koenekoop
Journal:  Ophthalmic Genet       Date:  2017-01-17       Impact factor: 1.803

3.  Amelioration of Neurosensory Structure and Function in Animal and Cellular Models of a Congenital Blindness.

Authors:  Ji Yun Song; Puya Aravand; Sergei Nikonov; Lanfranco Leo; Arkady Lyubarsky; Jeannette L Bennicelli; Jieyan Pan; Zhangyong Wei; Ivan Shpylchak; Pamela Herrera; Daniel J Bennett; Nicoletta Commins; Albert M Maguire; Jennifer Pham; Anneke I den Hollander; Frans P M Cremers; Robert K Koenekoop; Ronald Roepman; Patsy Nishina; Shangzhen Zhou; Wei Pan; Gui-Shuang Ying; Tomas S Aleman; Jimmy de Melo; Ilan McNamara; Junwei Sun; Jason Mills; Jean Bennett
Journal:  Mol Ther       Date:  2018-03-21       Impact factor: 11.454

4.  A mutation in IFT43 causes non-syndromic recessive retinal degeneration.

Authors:  Pooja Biswas; Jacque L Duncan; Muhammad Ali; Hiroko Matsui; Muhammad Asif Naeem; Pongali B Raghavendra; Kelly A Frazer; Heleen H Arts; Sheikh Riazuddin; Javed Akram; J Fielding Hejtmancik; S Amer Riazuddin; Radha Ayyagari
Journal:  Hum Mol Genet       Date:  2017-12-01       Impact factor: 6.150

5.  Screening of a large cohort of leber congenital amaurosis and retinitis pigmentosa patients identifies novel LCA5 mutations and new genotype-phenotype correlations.

Authors:  Donna S Mackay; Arundhati Dev Borman; Frans P M Cremers; Anthony T Moore; Robert K Koenekoop; Ruifang Sui; L Ingeborgh van den Born; Eliot L Berson; Louise A Ocaka; Alice E Davidson; John R Heckenlively; Kari Branham; Huanan Ren; Irma Lopez; Maleeha Maria; Maleeha Azam; Arjen Henkes; Ellen Blokland; Raheel Qamar; Andrew R Webster; Sten Andreasson; Elfride de Baere; Jean Bennett; Gerald J Chader; Wolfgang Berger; Irina Golovleva; Jacquie Greenberg; Anneke I den Hollander; Caroline C W Klaver; B Jeroen Klevering; Birgit Lorenz; Markus N Preising; Raj Ramsear; Lisa Roberts; Ronald Roepman; Klaus Rohrschneider; Bernd Wissinger
Journal:  Hum Mutat       Date:  2013-09-17       Impact factor: 4.878

6.  Identification of a novel LCA5 mutation in a Pakistani family with Leber congenital amaurosis and cataracts.

Authors:  Adeel Ahmad; Shakeela Daud; Naseebullah Kakar; Gudrun Nürnberg; Peter Nürnberg; Masroor Ellahi Babar; Michaela Thoenes; Christian Kubisch; Jamil Ahmad; Hanno Jörn Bolz
Journal:  Mol Vis       Date:  2011-07-16       Impact factor: 2.367

7.  Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis.

Authors:  Vedam Lakshmi Ramprasad; Nagasamy Soumittra; Derek Nancarrow; Parveen Sen; Martin McKibbin; Grange A Williams; Tharigopala Arokiasamy; Praveena Lakshmipathy; Chris F Inglehearn; Govindasamy Kumaramanickavel
Journal:  Mol Vis       Date:  2008-03-10       Impact factor: 2.367

8.  Treatment Potential for LCA5-Associated Leber Congenital Amaurosis.

Authors:  Katherine E Uyhazi; Puya Aravand; Brent A Bell; Zhangyong Wei; Lanfranco Leo; Leona W Serrano; Denise J Pearson; Ivan Shpylchak; Jennifer Pham; Vidyullatha Vasireddy; Jean Bennett; Tomas S Aleman
Journal:  Invest Ophthalmol Vis Sci       Date:  2020-05-11       Impact factor: 4.799

Review 9.  Voretigene Neparvovec and Gene Therapy for Leber's Congenital Amaurosis: Review of Evidence to Date.

Authors:  Srikanta Kumar Padhy; Brijesh Takkar; Raja Narayanan; Pradeep Venkatesh; Subhadra Jalali
Journal:  Appl Clin Genet       Date:  2020-11-25

10.  Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: retained photoreceptors adjacent to retinal disorganization.

Authors:  Samuel G Jacobson; Tomas S Aleman; Artur V Cideciyan; Alexander Sumaroka; Sharon B Schwartz; Elizabeth A M Windsor; Malgorzata Swider; Waldo Herrera; Edwin M Stone
Journal:  Mol Vis       Date:  2009-06-02       Impact factor: 2.367

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