Literature DB >> 17666886

Clinical aspects of hereditary hearing loss.

Amit Kochhar1, Michael S Hildebrand, Richard J H Smith.   

Abstract

Hearing loss is an etiologically diverse condition with many disease-related complications and major clinical, social, and quality of life implications. As the rate of acquired hearing loss secondary to environmental causes decreases and improvements in the diagnosis of abnormalities occur, the significance of genetic factors that lead to deafness increases. Advancements in molecular biology have led to improved detection and earlier intervention in patients with hearing loss. Subsequently, earlier implementation of educational services and cochlear implant technology in patients with profound hearing loss now results in superior communication skills and enhanced language development. The aim of this review is to provide a comprehensive framework underlying the causes of hearing impairment and to detail the clinical management for patients with hereditary hearing loss.

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Year:  2007        PMID: 17666886     DOI: 10.1097/gim.0b013e3180980bd0

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  32 in total

Review 1.  Genetics of hearing loss: where are we standing now?

Authors:  Hossein Mahboubi; Sami Dwabe; Matthew Fradkin; Virginia Kimonis; Hamid R Djalilian
Journal:  Eur Arch Otorhinolaryngol       Date:  2012-01-05       Impact factor: 2.503

2.  Effects of genetic correction on the differentiation of hair cell-like cells from iPSCs with MYO15A mutation.

Authors:  J-R Chen; Z-H Tang; J Zheng; H-S Shi; J Ding; X-D Qian; C Zhang; J-L Chen; C-C Wang; L Li; J-Z Chen; S-K Yin; J-Z Shao; T-S Huang; P Chen; M-X Guan; J-F Wang
Journal:  Cell Death Differ       Date:  2016-02-26       Impact factor: 15.828

3.  Special issues for the 55th Inner Ear Biology Workshop 06.-08.09.2018 in Berlin : Basic research and clinical aspects-translational aspects of hearing research.

Authors:  B Mazurek; M Knipper; E Biesinger; H Schulze
Journal:  HNO       Date:  2019-06       Impact factor: 1.284

4.  Extralabyrinthine manifestations of DFNA9.

Authors:  Andrew A McCall; Fred H Linthicum; Jennifer T O'Malley; Joe C Adams; Saumil N Merchant; Marc K Bassim; Robert Gellibolian; Jose N Fayad
Journal:  J Assoc Res Otolaryngol       Date:  2010-11-04

5. 

Authors:  Daniel Newsted; Emily Rosen; Bonnie Cooke; Michael M Beyea; Matthew T W Simpson; Jason A Beyea
Journal:  Can Fam Physician       Date:  2020-11       Impact factor: 3.275

6.  Cochlear Implantation in Congenital Long-QT Syndrome: A Comprehensive Study.

Authors:  Ronald Anto; Sudha Maheswari; Senthil Vadivu; Mohan Kameswaran
Journal:  J Int Adv Otol       Date:  2019-12       Impact factor: 1.017

Review 7.  Ethical and social implications of genetic testing for communication disorders.

Authors:  Kathleen S Arnos
Journal:  J Commun Disord       Date:  2008-03-25       Impact factor: 2.288

8.  Correlation between GJB2 mutations and audiological deficits: personal experience.

Authors:  Pasqualina M Picciotti; Roberta Pietrobono; Giovanni Neri; Gaetano Paludetti; Anna Rita Fetoni; Francesca Cianfrone; Maria Grazia Pomponi
Journal:  Eur Arch Otorhinolaryngol       Date:  2008-07-31       Impact factor: 2.503

Review 9.  Approach to hearing loss.

Authors:  Daniel Newsted; Emily Rosen; Bonnie Cooke; Michael M Beyea; Matthew T W Simpson; Jason A Beyea
Journal:  Can Fam Physician       Date:  2020-11       Impact factor: 3.275

10.  A claudin-9-based ion permeability barrier is essential for hearing.

Authors:  Yoko Nakano; Sung H Kim; Hyoung-Mi Kim; Joel D Sanneman; Yuzhou Zhang; Richard J H Smith; Daniel C Marcus; Philine Wangemann; Randy A Nessler; Botond Bánfi
Journal:  PLoS Genet       Date:  2009-08-21       Impact factor: 5.917

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