What’s the connection between Leber Congenital Amaurosis and the CEP290 gene?

Leber congenital amaurosis (LCA) is the most common cause of inherited childhood blindness, as roughly 3 out of 100,000 children around the world are affected by the disorder, which has similarities to retinitis pigmentosa.
The CEP290 gene provides instructions for making a protein that is present in many types of cells, including in the eye's light receptor cells (photoreceptors).
To get a full overview of the LCA disease and CEP290 gene, visit: www.cyagen.com/us/en/communit...
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[@sumanlimbusongpangbay]

Dear sir, my daughter is suffering from LCA5 eye disfunction since when she was about 1 month and my baby is now about 15 months so please advise for the treatment. 🙏

[@loadnlock357]

Go to a doctor

[@harperjiang2639]

Tips: