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X-linked inheritance means that the faulty gene is located on the X chromosome, the larger of the two sex chromosomes.

Prof Mariya Moosajee at Moorfields Eye Hospital has asked us to share the message below about the clinical trial she is running. This trial is for a treatment that targets a particular section of the USH2A gene.

• News
• Usher syndrome

Genetic counsellors are specially trained healthcare professionals with extensive scientific knowledge who spend time talking to families living with inherited conditions.

Inherited progressive sight loss is caused by a range of rare genetic conditions. We specialise in those which affect the retina.

Genetic testing, usually via a blood sample, is used to try and identify which gene contains the fault that is causing an individual’s sight loss.

We always aim to provide a high standard of service to our community. If you are unhappy with any of our services it is important that you let us know.

Martin started volunteering for Retina UK in 2014 after retiring as a Chartered Civil Engineer.

• Case study - community
• Audio
• Written

Inside this edition, set yourself a challenge in 2024, plus find out about our brand new lottery.

• Look Forward
• Audio
• Written

Giving a regular monthly or quarterly donation of any amount is a wonderful way to help Retina UK support the inherited sight loss community.

Saturday 18 May, 11.00am - 1.00pm - Via Zoom - Guest speaker Rory Field, CEO of London based charity, Metro Blind Sport.

• Local peer support group