Case report: Surgical and clinical results in bilateral lenticonus due to Alport syndrome
Esen Çakmak-Cengiz, Fadime Karaman-Atasever, Ertuğrul Can

TL;DR
This case report describes successful eye surgery in a man with Alport syndrome, a genetic disorder affecting the eyes, kidneys, and hearing.
Contribution
The paper presents a successful surgical approach for bilateral anterior lenticonus in Alport syndrome using phacoemulsification and IOL implantation.
Findings
Phacoemulsification and IOL implantation achieved optimal vision without capsular rupture in a patient with Alport syndrome.
The SRK-T formula provided accurate IOL calculation for successful postoperative refraction.
Careful surgical technique minimized complications in managing anterior lenticonus due to Alport syndrome.
Abstract
Alport syndrome (AS) is a genetic disease characterized by hereditary nephritis, sensorineural hearing loss, and ocular anomalies. The most common ocular findings associated with AS include anterior lenticonus, retinal dot-fleck configuration, and corneal posterior polymorphism. Anterior lenticonus is 8 times more common in men with AS than in women. This case report evaluated the clinical and optical results obtained after phacoemulsification (PHACO) surgery and intraocular lens (IOL) implantation performed for bilateral anterior lenticonus due to AS. A 35-year-old male patient had complained of progressively decreasing vision for 10 years. The patient’s ophthalmologic examination revealed bilateral anterior lenticonus and nuclear sclerosis. Continuous curvilinear capsulorhexis was applied in the anterior capsulorhexis method. Phacoemulsification surgery was performed using a…
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Taxonomy
TopicsCell Adhesion Molecules Research · Ocular Disorders and Treatments · Glaucoma and retinal disorders
