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Genetic analysis of patients with primary congenital glaucoma.

International ophthalmology - 1 Jul 2021

Ava Sedat, Demirtaş Atılım Armağan, Karahan Mine, Erdem Seyfettin, Oral Diclehan, Keklikçi Uğur

Abstract excerpt

PURPOSE: To determine the common gene mutation in patients with primary congenital glaucoma (PCG) in the Southeast region of Turkey via genetic analysis and to evaluate whether there were other gene mutations in these patients. METHODS: A total of 25 patients with PCG were included in this study. We performed sequence analysis including all exons of cytochrome p450 1B1 (CYP1B1), myocilin (MYOC), forkhead box C1...

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PMID: 33745036
DOI: 10.1007/s10792-021-01815-z

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