The disease is more frequent in healthy middleaged females aged 15-50 and can be preceded by a flu-like illness.
MEWDS classically manifests with multiple, whitish lesions located deep in the central area of the retina (macula), appearing as white dots.
The anterior part of the eye is usually not involved.
Mild inflammation of the vitreous (the jelly-like structure which fills the posterior cavity of the eye) which is known as vitiritis, and inflammatory involvement of the retinal vessels and optic disc can be detected.
An afferent pupillary defect, in which the pupil of the affected eye responds differently to light stimuli, can be present.
The white dots spontaneously resolve over a period of months.
There are no diagnostic laboratory tests and the clinical presentation of MEWDS is usually sufficient to confirm the diagnosis.
Dye tests, including fundus fluorescein angiography and indocyanine green angiography, are sometimes carried out to confirm the clinical suspicion. The retinal function can be measured by special tests, including visual fields and electrodiagnostic tests.
he clinical course of MEWDS is short and most patients recover nearly complete over a period of months.
However, flashing of lights and scotomas may last longer. Recurrences are uncommon.
Contact
Ilaria Testi
The London Clinic Eye Centre
119 Harley Street
London W1G 6AU
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