Question
My child is just a few months old, and recently we’ve noticed that the baby doesn’t seem to be looking at things, and it looks a bit like what others say is ‘crossed eyes.’ The hospital examination said it’s congenital blindness, but how could it be congenital? I’m especially worried. I want to get some help?
Answer
Firstly, it’s important to understand the cause of bilateral blindness. If it’s due to a genetic mutation, consider that many blind genes are located on the Y chromosome. It is recommended that you consult with an ophthalmologist for a definitive diagnosis of the cause of blindness. If it’s due to genetic inheritance, the likelihood of blindness in boys increases. It is advisable to consider this carefully and combine gene therapy. There are many causes of congenital blindness, such as incomplete development of the visual system, congenital glaucoma, and congenital cataracts, all of which can lead to poor vision in children. It is recommended that if parents notice that their child has poor vision, they should seek medical attention promptly to avoid delaying the condition.