Dental skeletal retinal anomaly · MIA3-related anomaly · DSRA syndrome · Zahn-Skelett-Netzhaut-Anomalie · MIA3-related dental-skeletal-retinal anomaly · Dental skeletal retinal syndrome · MIA3-associated DSRA · Dental-sketelal-retinal anomaly
Dentale-skeletale-retinale Anomalie (DSRA) is a severe, inherited systemic disease that affects multiple organ systems, specifically the teeth, bones, and the retina, which is the light-sensitive tissue at the back of the eye. It is caused by a genetic mutation that disrupts the normal development and structure of these essential tissues. This disruption prevents the skeleton, teeth, and eyes from forming and functioning properly.
Symptoms typically become noticeable in puppyhood. Owners may observe abnormally discolored, brittle teeth, stunted or delayed bone growth, and a progressive loss of vision that eventually leads to blindness.
There is no cure for this condition, and treatment is limited to supportive care to manage symptoms. Lifelong management and palliative care typically cost between 1,000 and 4,000 EUR, though the severe progression of the disease often leads to early euthanasia.
Estimated range of typical treatment cost. Actual cost depends on severity, clinic and region.
More conditions affecting the Eyes.