TGFB1 And LAMA1 Gene Polymorphisms in High Myopia

Status Completed

Clinical Trial Summary

The investigators aimed to investigate TGFB1 and LAMA1 gene polymorphisms in children with high myopia in order to determine the genetic basis of large myopic shifts causing severe visual impairment and complications.

Seventy-four children with high myopia (≥6 diopters [D]; study group) and 77 emmetropic children (±0.5D; control group) were included. Genetic and polymorphism analyses were performed in the Medical Genetics Laboratory using DNA purified from the patients' blood samples.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03451877
Study type	Interventional
Source	Ege University
Contact
Status	Completed
Phase	N/A
Start date	December 1, 2012
Completion date	June 1, 2017

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