Congenital blindness

Human eye anatomy

Congenital blindness refers to blindness present at birth.[1] Congenital blindness is sometimes used interchangeably with "Childhood Blindness." However, current literature has various definitions of both terms. Childhood blindness encompasses multiple diseases and conditions present in ages up to 16 years old, which can result in permanent blindness or severe visual impairment over time.[2] Congenital blindness is a hereditary disease and can be treated by gene therapy. Visual loss in children or infants can occur either at the prenatal stage (during the time of conception or intrauterine period) or postnatal stage (immediately after birth).[3] There are multiple possible causes of congenital blindness. In general, 60% of congenital blindness cases are contributed from prenatal stage and 40% are contributed from inherited disease.[4] However, most of the congenital blindness cases show that it can be avoidable or preventable with early treatment.[5]

  1. ^ "Congenital blindness (Concept Id: C0005754) - MedGen - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2023-07-27.
  2. ^ Khandekar R (July 2008). "Visual disabilities in children including childhood blindness". Middle East African Journal of Ophthalmology. 15 (3): 129–134. doi:10.4103/0974-9233.51988. PMC 3040917. PMID 21369469.
  3. ^ "WHO Technical Consultation on Postpartum Care", WHO Technical Consultation on Postpartum and Postnatal Care, World Health Organization, 2010, retrieved 2023-08-01
  4. ^ "Genetic Eye Disorders & Blindness Causes | Cleveland Clinic: Health Library". Cleveland Clinic. Retrieved 2019-04-14.
  5. ^ "Blindness (Vision Impairment): Types, Causes and Treatment". Cleveland Clinic. Retrieved 2023-08-01.