The risk factors for Acute Idiopathic Blind Spot Enlargement Syndrome may include:
It is important to note that having a risk factor does not mean that one will get the condition. A risk factor increases one’s chances of getting a condition compared to an individual without the risk factors. Some risk factors are more important than others.
Also, not having a risk factor does not mean that an individual will not get the condition. It is always important to discuss the effect of risk factors with your healthcare provider.
The cause of Acute Idiopathic Blind Spot Enlargement Syndrome is not well understood.
AIBSE Syndrome is believed to be a part of primary inflammatory choriocapillaropathies (PICCP) that form a spectrum of disorders which include white dot syndromes.
The signs and symptoms of Acute Idiopathic Blind Spot Enlargement Syndrome may vary between individuals and may include:
Acute Idiopathic Blind Spot Enlargement Syndrome may be diagnosed by the following observations and tests:
A differential diagnosis to eliminate other conditions may be considered, before arriving at a definitive diagnosis. These may include:
Many clinical conditions may have similar signs and symptoms. Your healthcare provider may perform additional tests to rule out other clinical conditions to arrive at a definitive diagnosis.
The complications of Acute Idiopathic Blind Spot Enlargement Syndrome may include:
The treatment of Acute Idiopathic Blind Spot Enlargement Syndrome is not well-defined. However, the following may be considered:
Currently, there are no methods to prevent Acute Idiopathic Blind Spot Enlargement Syndrome.
It is reported that the prognosis of the Acute Idiopathic Blind Spot Enlargement Syndrome is generally good in a majority of cases, since the condition is self-limiting.
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