Literature DB >> 28685406

Leber's Congenital Amaurosis and Gene Therapy.

Brijesh Takkar1, Pooja Bansal1, Pradeep Venkatesh2.   

Abstract

Retinal blindness is an important cause of pediatric visual loss. Leber's congenital amaurosis (LCA) is one of these causes, often wrongly included in the spectrum of retinitis pigmentosa. The disease has become the center of research after initial reports of success in management with gene therapy. This review discusses in brief the clinical presentation and investigative modalities used in LCA. Further, the road to gene discovery and details of currently applied gene therapy are presented. LCA is one of the first successfully managed human diseases and offers an entirely new dimension in ocular therapeutics.

Entities:  

Keywords:  Gene therapy; Leber's congenital amaurosis; Pediatric blindness

Mesh:

Year:  2017        PMID: 28685406     DOI: 10.1007/s12098-017-2394-1

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  36 in total

1.  Mutations in RPE65 cause Leber's congenital amaurosis.

Authors:  F Marlhens; C Bareil; J M Griffoin; E Zrenner; P Amalric; C Eliaou; S Y Liu; E Harris; T M Redmond; B Arnaud; M Claustres; C P Hamel
Journal:  Nat Genet       Date:  1997-10       Impact factor: 38.330

Review 2.  [Gene therapy for hereditary ophthalmological diseases: Advances and future perspectives].

Authors:  Óscar Francisco Chacón-Camacho; Aline Astorga-Carballo; Juan Carlos Zenteno
Journal:  Gac Med Mex       Date:  2015 Jul-Aug       Impact factor: 0.302

Review 3.  Seven hereditary syndromes with pigmentary retinopathy. A review and differential diagnosis.

Authors:  A Cantani; P Bellioni; G Bamonte; F Salvinelli; M T Bamonte
Journal:  Clin Pediatr (Phila)       Date:  1985-10       Impact factor: 1.168

Review 4.  Review and update on the molecular basis of Leber congenital amaurosis.

Authors:  Oscar Francisco Chacon-Camacho; Juan Carlos Zenteno
Journal:  World J Clin Cases       Date:  2015-02-16       Impact factor: 1.337

5.  Correlation of ultra-widefield fundus autofluorescence patterns with the underlying genotype in retinal dystrophies and retinitis pigmentosa.

Authors:  George Trichonas; Elias I Traboulsi; Justis P Ehlers
Journal:  Ophthalmic Genet       Date:  2016-11-23       Impact factor: 1.803

6.  Autosomal-dominant Leber Congenital Amaurosis Caused by a Heterozygous CRX Mutation in a Father and Son.

Authors:  Karthikeyan Arcot Sadagopan; Robert Battista; Rosanne B Keep; Jenina E Capasso; Alex V Levin
Journal:  Ophthalmic Genet       Date:  2013-10-04       Impact factor: 1.803

7.  Targeting iodothyronine deiodinases locally in the retina is a therapeutic strategy for retinal degeneration.

Authors:  Fan Yang; Hongwei Ma; Joshua Belcher; Michael R Butler; T Michael Redmond; Sanford L Boye; William W Hauswirth; Xi-Qin Ding
Journal:  FASEB J       Date:  2016-09-13       Impact factor: 5.191

8.  Effect of gene therapy on visual function in Leber's congenital amaurosis.

Authors:  James W B Bainbridge; Alexander J Smith; Susie S Barker; Scott Robbie; Robert Henderson; Kamaljit Balaggan; Ananth Viswanathan; Graham E Holder; Andrew Stockman; Nick Tyler; Simon Petersen-Jones; Shomi S Bhattacharya; Adrian J Thrasher; Fred W Fitzke; Barrie J Carter; Gary S Rubin; Anthony T Moore; Robin R Ali
Journal:  N Engl J Med       Date:  2008-04-27       Impact factor: 91.245

9.  Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial.

Authors:  Albert M Maguire; Katherine A High; Alberto Auricchio; J Fraser Wright; Eric A Pierce; Francesco Testa; Federico Mingozzi; Jeannette L Bennicelli; Gui-shuang Ying; Settimio Rossi; Ann Fulton; Kathleen A Marshall; Sandro Banfi; Daniel C Chung; Jessica I W Morgan; Bernd Hauck; Olga Zelenaia; Xiaosong Zhu; Leslie Raffini; Frauke Coppieters; Elfride De Baere; Kenneth S Shindler; Nicholas J Volpe; Enrico M Surace; Carmela Acerra; Arkady Lyubarsky; T Michael Redmond; Edwin Stone; Junwei Sun; Jennifer Wellman McDonnell; Bart P Leroy; Francesca Simonelli; Jean Bennett
Journal:  Lancet       Date:  2009-10-23       Impact factor: 79.321

10.  Long-term effect of gene therapy on Leber's congenital amaurosis.

Authors:  James W B Bainbridge; Manjit S Mehat; Venki Sundaram; Scott J Robbie; Susie E Barker; Caterina Ripamonti; Anastasios Georgiadis; Freya M Mowat; Stuart G Beattie; Peter J Gardner; Kecia L Feathers; Vy A Luong; Suzanne Yzer; Kamaljit Balaggan; Ananth Viswanathan; Thomy J L de Ravel; Ingele Casteels; Graham E Holder; Nick Tyler; Fred W Fitzke; Richard G Weleber; Marko Nardini; Anthony T Moore; Debra A Thompson; Simon M Petersen-Jones; Michel Michaelides; L Ingeborgh van den Born; Andrew Stockman; Alexander J Smith; Gary Rubin; Robin R Ali
Journal:  N Engl J Med       Date:  2015-05-04       Impact factor: 91.245

View more
  5 in total

1.  Editorial: Pediatric Ophthalmology - Part II.

Authors:  Pradeep Venkatesh
Journal:  Indian J Pediatr       Date:  2018-02-09       Impact factor: 1.967

2.  Associations Between Fundus Types and Clinical Manifestations in Patients with RDH12 Gene Mutations.

Authors:  Jing Jin; Liang Liang; Kun Jin; Hai-Jiang Zhang; Rong Liu; Yin Shen
Journal:  Brain Topogr       Date:  2022-01-10       Impact factor: 4.275

Review 3.  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

4.  Oculodigital Sign: A Clinical Clue for Diagnosis.

Authors:  Sangeetha Yoganathan; Madhan Kumar; Deepa John; Sumita Danda; Samuel P Oommen; Sayli B Umakant; Maya Thomas
Journal:  Ann Indian Acad Neurol       Date:  2022-05-03       Impact factor: 1.714

5.  Lutein and Zeaxanthin Isomers Reduce Photoreceptor Degeneration in the Pde6b rd10 Mouse Model of Retinitis Pigmentosa.

Authors:  Minzhong Yu; Weiming Yan; Craig Beight
Journal:  Biomed Res Int       Date:  2018-12-17       Impact factor: 3.411

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.