FIELD: medicine. SUBSTANCE: method involves intravitreally expanding the retina by applying perfluororganic substance and fixing rupture edge to tunicae bulbi by means of magnetic device. One rupture zone is coated with internal magnetic sealing membrane from polymer material. The sealing membrane is introduced through the flat part of the ciliary body and fixed in the vicinity of the extraocular magnetic sealing membrane. The sealing membrane is modeled corresponding to rupture configuration so that its sizes exceed by 20-60 % the defect area. Intravitreal barrier argon laser retina coagulation is carried out. EFFECT: positive anatomic result.
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