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The relationship of retinopathy of prematurity with brain-derivated neurotrophic factor, vascular endotelial growth factor-A, endothelial PAD domain protein 1 and nitric oxide synthase 3 gene polymorphisms.

Serdar IlguyOguz CilingirMustafa Deger BilgecOnur OzalpEbru Erzurumluoglu GokalpSerap ArslanNeslihan TekinOzge AydemirNazmiye ErolErtugrul ColakHuseyin Gursoy
Published in: Ophthalmic genetics (2021)
Considering the results of our study, it was seen that besides the known environmental and demographic factors in ROP pathogenesis, genetic predisposition also had an effect on the clinic and course of ROP. Polymorphisms of VEGFA rs2010963 and rs3025039, EPAS1 rs13419896, NOS3 rs2070744 were found to be associated with severe ROP. More studies involving different populations cases are needed to confirm these findings and enlighten the etiology of ROP.
Keyphrases
  • nitric oxide synthase
  • growth factor
  • nitric oxide
  • primary care
  • early onset
  • white matter
  • resting state
  • dna methylation
  • amino acid
  • climate change
  • functional connectivity
  • life cycle
  • genetic diversity
  • cerebral ischemia