Abstract
The authors describe two cases of idiopathic uveal effusion syndrome,
in one instance affecting consecutively both eyes, in the second
patient the finding is unilateral so far. In the female patient with
the bilateral finding reattachment of the retina and improvement
of the visual acuity developed only after surgery (sclerotomy). The
second patient, where the disease was detected only accidentally,
is so far only under observation. The authors discuss the causes
of this rare disease, the variability of clinical symptoms, diagnostic
and therapeutic possibilities.
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