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Weill syndrome is a rare hereditary disease that manifests itself in the form of abnormalities in the development of the eyeball and optic nerves. It was described by the French ophthalmologist Georges Weill and the English neurologist William J. Adie in 1897.

Symptoms of Weill syndrome can appear in various forms. In some cases, patients experience significant pupil constriction and iris atrophy. This can lead to blurred vision and decreased visual acuity. In other cases, there is a disruption in the development of the optic nerve, which leads to decreased sensitivity to light and loss of vision.

Treatment of Weill's syndrome depends on its form and severity. In some cases, surgery may be required to correct eye abnormalities. Drug therapy may also be prescribed to improve vision and reduce symptoms.

Weill syndrome is a rare disease that can only be diagnosed with a thorough examination of the patient. However, if you suspect the presence of this syndrome, you should consult an ophthalmologist for diagnosis and appropriate treatment.

Weill-Rey-Adie syndrome (or simply Weill's syndrome) is a rare congenital disorder that causes visual impairment and can lead to blindness. The name of the disease comes from the names of three French and English doctors who described this disease at the beginning of the 20th century.

Weill's syndrome was first described by a Frenchman