Login / Signup

Variable Phenotype of Congenital Corneal Opacities in Biallelic CYP1B1 Pathogenic Variants.

Elena FrancoMeghal GagraniHannah L ScangaRaymond G AreauxCharleen T ChuKen K Nischal
Published in: Cornea (2023)
Congenital corneal opacities seen in biallelic CYP1B1 pathogenic variants have a variable phenotype. One is that commonly termed as Peters anomaly type 1 (with iridocorneal adhesions, with or without iridolenticular adhesions) and the other is a limbus-to-limbus opacity, termed CYP1B1 cytopathy. Clinicians should be aware of this phenotypic variability.
Keyphrases
  • copy number
  • intellectual disability
  • optical coherence tomography
  • wound healing
  • palliative care
  • autism spectrum disorder
  • dna methylation