Literature DB >> 23845030

Genetic testing for inherited ocular disease: delivering on the promise at last?

Rachel L Gillespie1, Georgina Hall, Graeme C Black.   

Abstract

Genetic testing is of increasing clinical utility for diagnosing inherited eye disease. Clarifying a clinical diagnosis is important for accurate estimation of prognosis, facilitating genetic counselling and management of families, and in the future will direct gene-specific therapeutic strategies. Often, precise diagnosis of genetic ophthalmic conditions is complicated by genetic heterogeneity, a difficulty that the so-called 'next-generation sequencing' technologies promise to overcome. Despite considerable counselling and ethical complexities, next-generation sequencing offers to revolutionize clinical practice. This will necessitate considerable adjustment to standard practice but has the power to deliver a personalized approach to genomic medicine for many more patients and enhance the potential for preventing vision loss.
© 2013 Royal Australian and New Zealand College of Ophthalmologists.

Entities:  

Keywords:  counselling; ethics; genetics; inherited eye disease; testing

Mesh:

Year:  2013        PMID: 23845030     DOI: 10.1111/ceo.12159

Source DB:  PubMed          Journal:  Clin Exp Ophthalmol        ISSN: 1442-6404            Impact factor:   4.207


  8 in total

1.  Identifying variation in models of care for the genomic-based diagnosis of inherited retinal dystrophies in the United Kingdom.

Authors:  M Eden; K Payne; C Jones; S J Wright; G Hall; M McAllister; G Black
Journal:  Eye (Lond)       Date:  2016-04-15       Impact factor: 3.775

Review 2.  Are we ready for genetic testing for primary open-angle glaucoma?

Authors:  Anthony P Khawaja; Ananth C Viswanathan
Journal:  Eye (Lond)       Date:  2018-01-30       Impact factor: 3.775

Review 3.  Navigating the current landscape of clinical genetic testing for inherited retinal dystrophies.

Authors:  Kristy Lee; Seema Garg
Journal:  Genet Med       Date:  2015-03-19       Impact factor: 8.822

Review 4.  Hereditary retinal eye diseases in childhood and youth affecting the central retina.

Authors:  Martin M Nentwich; Guenther Rudolph
Journal:  Oman J Ophthalmol       Date:  2013-09

5.  Diagnostic exome sequencing in 266 Dutch patients with visual impairment.

Authors:  Lonneke Haer-Wigman; Wendy Ag van Zelst-Stams; Rolph Pfundt; L Ingeborgh van den Born; Caroline Cw Klaver; Joke Bgm Verheij; Carel B Hoyng; Martijn H Breuning; Camiel Jf Boon; Anneke J Kievit; Virginie Jm Verhoeven; Jan Wr Pott; Suzanne Ceh Sallevelt; Johanna M van Hagen; Astrid S Plomp; Hester Y Kroes; Stefan H Lelieveld; Jayne Y Hehir-Kwa; Steven Castelein; Marcel Nelen; Hans Scheffer; Dorien Lugtenberg; Frans Pm Cremers; Lies Hoefsloot; Helger G Yntema
Journal:  Eur J Hum Genet       Date:  2017-02-22       Impact factor: 4.246

6.  Whole exome sequencing of a family revealed a novel variant in the CHM gene, c.22delG p.(Glu8Serfs*4), which co-segregated with choroideremia.

Authors:  Handong Dan; Tuo Li; Xinlan Lei; Xin Huang; Yiqiao Xing; Yin Shen
Journal:  Biosci Rep       Date:  2020-05-29       Impact factor: 3.840

Review 7.  Unsolved challenges of clinical whole-exome sequencing: a systematic literature review of end-users' views.

Authors:  Gabrielle Bertier; Martin Hétu; Yann Joly
Journal:  BMC Med Genomics       Date:  2016-08-11       Impact factor: 3.063

Review 8.  Genetic counselling in the era of genomic medicine.

Authors:  Christine Patch; Anna Middleton
Journal:  Br Med Bull       Date:  2018-06-01       Impact factor: 4.291

  8 in total

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