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Pathological changes in the choroid, the \u201cretinal pigment epithelium \u2014 Bruch\u2019s membrane\u201d complex, and the neurosensory retina, identified using fundus photography, short-wavelength autofluorescence, optical coherence tomography (OCT), and OCT angiography, are described as nonspecific in nature. Given the verification of renal thrombotic microangiopathy by nephrobiopsy in this clinical case, the likely pathogenic mechanism underlying the observed chorioretinopathy manifestations is chronic ocular thrombotic microangiopathy.<\/jats:p>","DOI":"10.17116\/oftalma202414006190","type":"journal-article","created":{"date-parts":[[2024,12,28]],"date-time":"2024-12-28T05:49:26Z","timestamp":1735364966000},"page":"90","source":"Crossref","is-referenced-by-count":1,"title":["Retinopathy associated with thrombotic microangiopathy of mixed origin (case report)"],"prefix":"10.17116","volume":"140","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-4043-456X","authenticated-orcid":false,"given":"Yu.N.","family":"Yusef","sequence":"first","affiliation":[{"name":"Krasnov Research Institute of Eye Diseases","place":["Moscow, Russia"]},{"name":"I.M. 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