Granular corneal dystrophy is a rare genetic eye condition that affects the clarity of the cornea. It is caused by the buildup of protein clusters called granules in the cornea, leading to vision impairment. The condition can affect both eyes, but it can also affect only one eye, such as the left eye.
Granular corneal dystrophy is usually diagnosed in the teenage years or early adulthood, and the symptoms can vary depending on the severity of the condition. In some cases, the granules can cause haze or clouding in the cornea, leading to blurred vision. Patients may also experience sensitivity to light, eye irritation, and discomfort.
Granular corneal dystrophy is a progressive condition, and early diagnosis and treatment can help to preserve vision and prevent further vision loss. If you are experiencing any symptoms associated with granular corneal dystrophy, it is important to consult with an ophthalmologist for a comprehensive eye exam and diagnosis.
Overall, granular corneal dystrophy can have a significant impact on a patient's vision and quality of life. However, with proper management and treatment, patients can maintain their vision and live a fulfilling life.
Granular corneal dystrophy is a rare genetic eye disorder that causes the accumulation of protein deposits in the cornea, leading to vision loss. While there is no cure for this condition, there are various treatment options available to manage the symptoms and slow down the progression of the disease.