Literature DB >> 24138041

Deprivation amblyopia and congenital hereditary cataract.

Behzad Mansouri1, Rebecca C Stacy, Joshua Kruger, Dean M Cestari.   

Abstract

Amblyopia is a neurodevelopmental disorder of vision associated with decreased visual acuity, poor or absent stereopsis, and suppression of information from one eye.(1,2) Amblyopia may be caused by strabismus (strabismic amblyopia), refractive error (anisometropic amblyopia), or deprivation from obstructed vision (deprivation amblyopia). 1 In the developed world, amblyopia is the most common cause of childhood visual impairment, 3 which reduces quality of life 4 and also almost doubles the lifetime risk of legal blindness.(5, 6) Successful treatment of amblyopia greatly depends on early detection and treatment of predisposing disorders such as congenital cataract, which is the most common cause of deprivational amblyopia. Understanding the genetic causes of congenital cataract leads to more effective screening tests, early detection and treatment of infants and children who are at high risk for hereditary congenital cataract.

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Year:  2013        PMID: 24138041     DOI: 10.3109/08820538.2013.825289

Source DB:  PubMed          Journal:  Semin Ophthalmol        ISSN: 0882-0538            Impact factor:   1.975


  4 in total

Review 1.  RNA-binding proteins in eye development and disease: implication of conserved RNA granule components.

Authors:  Soma Dash; Archana D Siddam; Carrie E Barnum; Sarath Chandra Janga; Salil A Lachke
Journal:  Wiley Interdiscip Rev RNA       Date:  2016-05-01       Impact factor: 9.957

2.  The Tudor-domain protein TDRD7, mutated in congenital cataract, controls the heat shock protein HSPB1 (HSP27) and lens fiber cell morphology.

Authors:  Carrie E Barnum; Salma Al Saai; Shaili D Patel; Catherine Cheng; Deepti Anand; Xiaolu Xu; Soma Dash; Archana D Siddam; Lisa Glazewski; Emily Paglione; Shawn W Polson; Shinichiro Chuma; Robert W Mason; Shuo Wei; Mona Batish; Velia M Fowler; Salil A Lachke
Journal:  Hum Mol Genet       Date:  2020-07-29       Impact factor: 6.150

3.  Case Report: A Novel Mutation in the CRYGD Gene Causing Congenital Cataract Associated with Nystagmus in a Chinese Family.

Authors:  Yunxia Gao; Xiang Ren; Xiangyu Fu; Yu Lin; Lirong Xiao; Xiaoyue Wang; Naihong Yan; Ming Zhang
Journal:  Front Genet       Date:  2022-02-10       Impact factor: 4.599

Review 4.  Prevalence of Pediatric Cataract in Asia: A Systematic Review and Meta-Analysis.

Authors:  Muhammad Ali Tariq; Qazi Shurjeel Uddin; Bilal Ahmed; Shehryar Sheikh; Uzair Ali; Ashar Mohiuddin
Journal:  J Curr Ophthalmol       Date:  2022-07-26
  4 in total

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