Literature DB >> 8694131

Early diagnosis of Usher syndrome in infants and children.

N M Young1, M B Mets, T C Hain.   

Abstract

The electroretinogram (ERG) is the only test currently available that has the potential to identify patients with Usher syndrome before onset of fundoscopic and visual abnormalities. The ERG is a noninvasive technique that can diagnose retinitis pigmentosa via measurement of corneal-retinal potentials. Forty-seven children with bilateral severe to profound sensorineural hearing loss were evaluated. Usher syndrome was diagnosed in five children, all of whom subsequently underwent cochlear implantation. We have found that accurate diagnosis of Usher syndrome in infants and young children is possible via ERG. Benefits of early diagnosis include timely counseling regarding genetic issues, educational and vocational placement, and cochlear implantation. For this reason we recommend that all newly identified children with bilateral severe to profound sensorineural hearing loss undergo ERG testing.

Entities:  

Mesh:

Year:  1996        PMID: 8694131

Source DB:  PubMed          Journal:  Am J Otol        ISSN: 0192-9763


  8 in total

1.  Usher syndrome in the city of Birmingham--prevalence and clinical classification.

Authors:  C I Hope; S Bundey; D Proops; A R Fielder
Journal:  Br J Ophthalmol       Date:  1997-01       Impact factor: 4.638

2.  A novel D458V mutation in the SANS PDZ binding motif causes atypical Usher syndrome.

Authors:  E Kalay; A P M de Brouwer; R Caylan; S B Nabuurs; B Wollnik; A Karaguzel; J G A M Heister; H Erdol; F P M Cremers; C W R J Cremers; H G Brunner; H Kremer
Journal:  J Mol Med (Berl)       Date:  2005-11-08       Impact factor: 4.599

3.  Variations in genetic assessment and recurrence risks quoted for childhood deafness: a survey of clinical geneticists.

Authors:  M J Parker; H Fortnum; I D Young; A C Davis
Journal:  J Med Genet       Date:  1999-02       Impact factor: 6.318

4.  Outcomes of cochlear implantation in children with Usher syndrome: a long-term observation.

Authors:  Agnieszka Remjasz-Jurek; Pedro Clarós; Astrid Clarós-Pujol; Carmen Pujol; Andrés Clarós
Journal:  Eur Arch Otorhinolaryngol       Date:  2022-10-15       Impact factor: 3.236

5.  CRISPR/Cas9 editing of the MYO7A gene in rhesus macaque embryos to generate a primate model of Usher syndrome type 1B.

Authors:  Junghyun Ryu; John P Statz; William Chan; Fernanda C Burch; John V Brigande; Beth Kempton; Edward V Porsov; Lauren Renner; Trevor McGill; Benjamin J Burwitz; Carol B Hanna; Martha Neuringer; Jon D Hennebold
Journal:  Sci Rep       Date:  2022-06-16       Impact factor: 4.996

6.  Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus.

Authors:  Sadaf Naz; Chantal M Giguere; David C Kohrman; Kristina L Mitchem; Saima Riazuddin; Robert J Morell; Arabandi Ramesh; Srikumari Srisailpathy; Dilip Deshmukh; Sheikh Riazuddin; Andrew J Griffith; Thomas B Friedman; Richard J H Smith; Edward R Wilcox
Journal:  Am J Hum Genet       Date:  2002-07-24       Impact factor: 11.025

Review 7.  Retinal remodeling in human retinitis pigmentosa.

Authors:  B W Jones; R L Pfeiffer; W D Ferrell; C B Watt; M Marmor; R E Marc
Journal:  Exp Eye Res       Date:  2016-03-26       Impact factor: 3.467

8.  Dark-adapted threshold and electroretinogram for diagnosis of Usher syndrome.

Authors:  Lucia Ambrosio; Ronald M Hansen; Anne Moskowitz; Andrea Oza; Devon Barrett; Juliana Manganella; Genevieve Medina; Kosuke Kawai; Anne B Fulton; Margaret Kenna
Journal:  Doc Ophthalmol       Date:  2021-01-28       Impact factor: 2.379

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.