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Crystalline gene mutations in Turkish children with congenital cataracts.

International ophthalmology - 1 Aug 2021

Karahan Mine, Demirtaş Atılım Armağan, Erdem Seyfettin, Ava Sedat, Tekeş Selahattin, Keklikçi Uğur

Abstract excerpt

PURPOSE: To detect crystallin gene mutations in Turkish children with congenital cataracts. METHODS: The present study included 56 children (38 males and 18 females) who were diagnosed with congenital cataract in our ophthalmology clinic. The patients' blood samples were collected and sent to the medical genetics laboratory. The samples were assessed using the sequence analysis method, which covered all exons of...

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PMID: 33864186
DOI: 10.1007/s10792-021-01843-9

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