Wellbeing A-Z -Usher syndrome

Usher syndrome is a genetic disorder causing deaf blindness, affecting 1 in 25,000 people. It is inherited through a recessive gene from both parents. There are three types: Type 1 involves balance issues and early vision loss, Type 2 has no balance problems but leads to vision loss by age 20, and Type 3 shows symptoms in adulthood. Despite challenges, individuals with Usher syndrome can achieve academic success. Gene therapy offers hope for a cure, with recent successes in mice. Genetic screening and vitamin A supplementation may help manage the condition.

How does Usher syndrome impact the balance and mobility of affected children?

What role do genetics play in the inheritance of Usher syndrome?