Conditions / Eye

Leber congenital amaurosis 15

info · Eye · ICD-10: H35.5

A Leber congenital amaurosis that has_material_basis_in mutation in the TULP1 gene on chromosome 6p21.3.

Signs and symptoms

  • Constriction of peripheral visual field
  • Nyctalopia
  • Color vision defect
  • Slow pupillary light response
  • Hemeralopia
  • Nystagmus
  • Reduced visual acuity
  • Attenuation of retinal blood vessels
  • Myopia
  • Pigmentary retinopathy

Also known as: LCA15