June 27 was the start of International Deafblind Awareness Week.<\/p>\n
Usher Syndrome is one of the most common causes of deaf-blindness and this genetic disease is sadly under-diagnosed in young children.<\/p>
Children who are born with severe or profound loss of hearing are generally not checked for retinal visual loss and inadequate preparation is made to allow for later loss of vision.<\/p>\n
Usher Syndrome<\/a> occurs in three distinct forms, with type one being the most profound deafness.<\/p> The good news is that clinical trials are underway to replace a defective gene, the MYO7A gene, with a working copy of the gene in patients affected by Usher Syndrome type-1b.<\/p>\n Retina South Africa, the patient action group for people with genetic retinal degenerative conditions, has partnered with the University of Cape Town to identify Usher patients who may benefit from this new era of future treatments.<\/p>\n Usher type two and three patients are also encouraged to contact Retina South Africa, who will facilitate gene testing to identify the precise gene causing the Usher Syndrome deaf-blindness.<\/p>\n International collaboration, coupled with more funding support, will ensure that these and other promising treatments are brought to South Africa.<\/p>\n \u201cOf the estimated 8 000 people in South Africa affected by Usher Syndrome, only a mere handful are registered with our foundation,\u201d said Claudette Medefindt, head of science for Retina South Africa<\/a>.<\/p>\n \u201cThirteen different gene mutations have already been associated with the three types of Usher Syndrome<\/a> and a genetic diagnosis is the first step towards future treatment.\u201d<\/p>\n <\/p>\n <\/p>\n