PA Medical News about Hearing Loss

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Genotype-Phenotype Correlation for DFNA22: Characterization of Non-Syndromic, Autosomal Dominant, Progressive Sensorineural Hearing Loss due to MYO6 Mutations
Audiology & Neuro-Otology, 11/05/09

Topsakal V et al. – This study describes the phenotype of 2 Belgian families with SNHL linked to DFNA22, both with a pathogenic change in the deafness gene MYO6. The phenotypes of all hitherto reported DFNA22 families with mutations in the MYO6 gene have been studied and compared. It seems that genetic defects that spare the motor domain of the myosin VI protein have a milder phenotype.

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Additional heterozygous 2507A>C mutation of WFS1 in progressive hearing loss at lower frequencies
The Laryngoscope, 11/05/09 Relevance Score: 68%

High incidence of hearing loss in long-term survivors of multisystem langerhans cell histiocytosis
Pediatric Blood & Cancer, 10/22/09 Relevance Score: 68%

Acoustic analysis of voice in cochlear implant recipients with post-meningitic hearing loss
Cochlear Implants International, 10/07/09 Relevance Score: 68%

Acute-Onset Unilateral Psychogenic Hearing Loss in Adults: Report of Six Cases and Diagnostic Pitfalls
Journal for Oto-Rhino-Laryngology, 10/23/09 Relevance Score: 67%

Diagnosing hearing problems
Paediatrics and Child Health, 10/06/09 Relevance Score: 67%