Literature DB >> 15752533

Sensorineural hearing loss in children.

Richard J H Smith1, James F Bale, Karl R White.   

Abstract

During the past three to four decades, the incidence of acquired sensorineural hearing loss (SNHL) in children living in more developed countries has fallen, as a result of improved neonatal care and the widespread implementation of immunisation programmes. The overall decrease has been accompanied by a relative increase in the proportion of inherited forms of SNHL. The contribution made by one gene in particular, GJB2, to the genetic load of SNHL has strongly affected the assessment and care of children with hearing loss. These changes in the incidence of SNHL have not been seen in children living in less developed countries, where the prevalence of consanguinity is high in many areas, and both genetic and acquired forms of SNHL are more common, particularly among children who live in poverty. Focused genetic counselling and health education might lead to a decrease in the prevalence of inherited SNHL in these countries. Establishment of vaccination programmes for several vaccine-preventable infectious diseases would reduce rates of acquired SNHL. Although the primary purpose of such programmes is the prevention of serious and in many cases fatal infections, a secondary benefit would be a reduction in disease-related complications such as SNHL that cause permanent disability in survivors.

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Year:  2005        PMID: 15752533     DOI: 10.1016/S0140-6736(05)71047-3

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  216 in total

Review 1.  Applications of targeted gene capture and next-generation sequencing technologies in studies of human deafness and other genetic disabilities.

Authors:  Xi Lin; Wenxue Tang; Shoeb Ahmad; Jingqiao Lu; Candice C Colby; Jason Zhu; Qing Yu
Journal:  Hear Res       Date:  2012-01-14       Impact factor: 3.208

2.  A low-cost exon capture method suitable for large-scale screening of genetic deafness by the massively-parallel sequencing approach.

Authors:  Wenxue Tang; Dong Qian; Shoeb Ahmad; Douglas Mattox; N Wendell Todd; Harrison Han; Shouting Huang; Yuhua Li; Yunfeng Wang; Huawei Li; Xi Lin
Journal:  Genet Test Mol Biomarkers       Date:  2012-04-05

3.  Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing.

Authors:  A Eliot Shearer; Adam P DeLuca; Michael S Hildebrand; Kyle R Taylor; José Gurrola; Steve Scherer; Todd E Scheetz; Richard J H Smith
Journal:  Proc Natl Acad Sci U S A       Date:  2010-11-15       Impact factor: 11.205

4.  The many faces of sensorineural hearing loss: one founder and two novel mutations affecting one family of mixed Jewish ancestry.

Authors:  Doron M Behar; Bella Davidov; Zippora Brownstein; Tamar Ben-Yosef; Karen B Avraham; Mordechai Shohat
Journal:  Genet Test Mol Biomarkers       Date:  2013-12-24

Review 5.  Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models.

Authors:  Emilie Hoang Dinh; Shoeb Ahmad; Qing Chang; Wenxue Tang; Benjamin Stong; Xi Lin
Journal:  Brain Res       Date:  2009-02-20       Impact factor: 3.252

6.  Genetic causes of moderate to severe hearing loss point to modifiers.

Authors:  Sadaf Naz; Ayesha Imtiaz; Ghulam Mujtaba; Azra Maqsood; Rasheeda Bashir; Ihtisham Bukhari; Muhammad R Khan; Memoona Ramzan; Amara Fatima; Atteeq U Rehman; Muddassar Iqbal; Taimur Chaudhry; Merete Lund; Carmen C Brewer; Robert J Morell; Thomas B Friedman
Journal:  Clin Genet       Date:  2016-10-06       Impact factor: 4.438

7.  [Hereditary hearing loss: Part 1: diagnostic overview and practical advice].

Authors:  W F Burke; T Lenarz; H Maier
Journal:  HNO       Date:  2013-04       Impact factor: 1.284

8.  Community-based infant hearing screening for early detection of permanent hearing loss in Lagos, Nigeria: a cross-sectional study.

Authors:  B O Olusanya; S L Wirz; L M Luxon
Journal:  Bull World Health Organ       Date:  2008-12       Impact factor: 9.408

9.  Mutations of TMC1 cause deafness by disrupting mechanoelectrical transduction.

Authors:  Hiroshi Nakanishi; Kiyoto Kurima; Yoshiyuki Kawashima; Andrew J Griffith
Journal:  Auris Nasus Larynx       Date:  2014-06-02       Impact factor: 1.863

10.  Restoration of hearing in the VGLUT3 knockout mouse using virally mediated gene therapy.

Authors:  Omar Akil; Rebecca P Seal; Kevin Burke; Chuansong Wang; Aurash Alemi; Matthew During; Robert H Edwards; Lawrence R Lustig
Journal:  Neuron       Date:  2012-07-26       Impact factor: 17.173

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