Literature DB >> 16114580

A genetic approach to the child with sensorineural hearing loss.

Heidi L Rehm1.   

Abstract

This article presents an overview of current topics related to the genetics of hearing loss. The review focuses on the approach toward a child with a sensorineural hearing loss of unknown etiology and the incorporation of genetic testing into the workup. Nongenetic causes of hearing loss are reviewed, as they are important in the differential diagnosis when considering a genetic basis for a child's hearing loss. The implications of universal newborn hearing screening and its implementation in many states are also addressed. Furthermore, important factors involved in the clinical diagnosis of the etiology of hearing loss, as well as factors relating to intervention and management of children with hearing loss are discussed. Finally, this review will consider genetic counseling for hearing loss and some of the issues important to the Deaf community.

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Year:  2005        PMID: 16114580     DOI: 10.1053/j.semperi.2004.12.002

Source DB:  PubMed          Journal:  Semin Perinatol        ISSN: 0146-0005            Impact factor:   3.300


  7 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.  Towards an etiologic diagnosis: assessing the patient with hearing loss.

Authors:  J Jerry; John S Oghalai
Journal:  Adv Otorhinolaryngol       Date:  2011-02-24

3.  Comprehensive diagnostic battery for evaluating sensorineural hearing loss in children.

Authors:  Jerry W Lin; Naweed Chowdhury; Avni Mody; Ross Tonini; Claudia Emery; Jody Haymond; John S Oghalai
Journal:  Otol Neurotol       Date:  2011-02       Impact factor: 2.311

Review 4.  Universal newborn hearing screening: methods and results, obstacles, and benefits.

Authors:  Katarzyna E Wroblewska-Seniuk; Piotr Dabrowski; Witold Szyfter; Jan Mazela
Journal:  Pediatr Res       Date:  2016-11-18       Impact factor: 3.756

5.  Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China.

Authors:  Hong Wu; Yong Feng; Lu Jiang; Qian Pan; Yalan Liu; Chang Liu; Chufeng He; Hongsheng Chen; Xueming Liu; Chang Hu; Yiqiao Hu; Lingyun Mei
Journal:  PLoS One       Date:  2016-03-28       Impact factor: 3.240

6.  Views of Syrian Mothers in Ankara on Infant Hearing Loss: Cross-sectional Survey.

Authors:  Diala Hussein; Hilal Dinçer D'Alessandro; Merve Özbal Batuk; Amar Ekhwan; Gonca Sennaroğlu
Journal:  Matern Child Health J       Date:  2022-09-05

7.  Factors influencing parental decision about genetics evaluation for their deaf or hard-of-hearing child.

Authors:  Christina G S Palmer; Jason T Lueddeke; Jin Zhou
Journal:  Genet Med       Date:  2009-04       Impact factor: 8.822

  7 in total

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