Articles

  • Jan 19, 2024 | onlinelibrary.wiley.com | Kate Leahy |Robyn Jamieson |John Grigg |Edward Lo-Cao

    1 INTRODUCTION The child who appears to not to see in the first year of life is a distressing finding for the family. Eye health professionals require a systematic approach to managing these children from both an ophthalmic perspective as well as the societal expectations. Significant anxiety accompanies this presentation partly due to the potential prospect of a lifetime of vision impairment for their child.

  • Dec 21, 2023 | onlinelibrary.wiley.com | Paul A Constable |Lynne Loh |John Grigg

    1 INTRODUCTION Familial Benign Fleck Retina (FBFR) (OMIM #228980) is an autosomal recessive condition caused by biallelic mutations in the gene PLA2G5 that encodes a family V phospholipase A2 which has multiple roles including signal transduction, phospholipid metabolism, and regulating phagocytosis.1-6 This rare condition has been observed predominantly in children and young adults that present with yellow to white symmetrical flecks bilaterally with otherwise normal acuity, visual fields,...

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