4. With reference to ‘Leber Congenital Amaurosis (LCA)’ consider the following statements :
- It is a rare genetic eye disorder where affected infants experience severe vision loss or blindness at birth.
- It is caused by a gene mutation that disrupts the proper function of the CEP290 protein, which is critical for vision.
- LCA affects approximately one in 40,000 people.
How many of the above pairs are correctly matched?