Non-syndromic Retinitis Pigmentosa Report

Non-syndromic Retinitis PigmentosaNon-syndromic Retinitis Pigmentosa is a rare genetic condition that causes progressive vision loss and can lead to blindness. This report analyzes genes associated with the condition, allowing for early detection and personalized treatment options for patients. This can benefit individuals who are experiencing symptoms of vision loss, as well as those with a family history of the condition, by providing them with information that can help guide their healthcare decisions.More than 75 genes analyzed It is recommended if: This report is recommended for individuals experiencing symptoms of vision loss or with a family history of Non-syndromic Retinitis Pigmentosa. The test can provide patients and their families with information that can help guide their healthcare decisions, including personalized treatment options and the potential for early detection. Early diagnosis can help prevent complications and improve patient outcomes. List of main conditions: