White dot syndromes: Difference between revisions
CSV import |
CSV import |
||
| Line 32: | Line 32: | ||
{{stub}} | {{stub}} | ||
{{No image}} | |||
Revision as of 21:06, 10 February 2025
White dot syndromes are a group of rare inflammatory diseases that affect the retina of the eye. They are characterized by the presence of white dots that appear in the posterior pole of the eye. These syndromes are often associated with inflammation and can cause severe vision loss if not treated promptly.
Overview
White dot syndromes are typically classified into several different types, including Birdshot chorioretinopathy, Multiple evanescent white dot syndrome, Acute posterior multifocal placoid pigment epitheliopathy, and others. Each of these conditions has its own unique set of symptoms and treatment options.
Symptoms
The symptoms of white dot syndromes can vary greatly depending on the specific type of syndrome. However, common symptoms often include blurred vision, floaters, and a decrease in visual field. In some cases, patients may also experience pain or discomfort in the eye.
Causes
The exact cause of white dot syndromes is currently unknown. However, it is believed that they may be caused by an autoimmune response that leads to inflammation in the retina. Some researchers also believe that certain viral infections may trigger the onset of these syndromes.
Diagnosis
Diagnosis of white dot syndromes typically involves a comprehensive eye exam, including a detailed examination of the retina. In some cases, additional tests such as fluorescein angiography or optical coherence tomography may be used to confirm the diagnosis.
Treatment
Treatment for white dot syndromes typically involves the use of anti-inflammatory medications to reduce inflammation in the retina. In severe cases, immunosuppressive drugs may be used to control the body's immune response.


