New research suggesting that age related hearing loss could one day be prevented has been welcomed by experts working for national charity Deafness Research UK, which hopes the research into a gene that ‘causes deafness' will lead to new insights into the causes of deafness at the genetic level and ultimately to the prospect of better treatments and cures. The Daily Mirror reported on 4 January 2012 that scientists have discovered that when the FGF20 gene was absent in mice, the animals appeared healthy - but had no hearing. In humans, the gene is found in the inner ear and has already been linked to inherited deafness.

Responding to the news, Dr David Furness, Deafness Research UK spokesman at the University of Keele said: "This research is great news because it identifies a gene that is vital to development of the delicate hair cells of the ear which are key to hearing in humans and animals. For those of us involved in research into the causes of deafness it could well prove to be a milestone in deafness research, and certainly identifies a key path for future studies to follow." 

Vivienne Michael, Chief Executive of Deafness Research UK, said: "We are hopeful that this latest research could open the door to understanding, preventing and eventually curing inherited hearing loss altogether. We need further funding to ensure that excellent research like this, which could ultimately improve the lives of millions, continues to be built upon by experts working in the field."

For further information on deafness and deafness-related conditions call freephone 0808 808 2222 or visit Deafness Research UK's website at www.deafnessresearch.org.uk