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A clinical case of a surgical treatment of complicated cataract in a patient with Hall–Hittner syndrome
2022
Clinical Practice
Variants of the CHD7 gene found in the OMIM 608892 genomic material are present in 8395% of patients suffering from the CHARGE syndrome. The aim of this report is to evaluate the clinical and functional results of cataract phacoemulsification with implantation of a toric intraocular lens in a patient with a very rare pathology HallHittner syndrome. Clinical case description: Under observation was patient V., who successfully underwent cataract phacoemulsification on the right eye with
doi:10.17816/clinpract106524
fatcat:akji2n5ckneafds3np6lg2zjra