Leber congenital amaurosis - Global Genes

Leber congenital amaurosis is an eye disorder that primarily affects the retina. People with this condition typically have severe visual impairment beginning in infancy. Other features include photophobia, involuntary movements of the eyes (nystagmus), and extreme farsightedness. The pupils also do not react normally to light. Additionally, the the cornea may be cone-shaped and abnormally thin.

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I’m a new visitor to Leber congenital amaurosis - Global Genes. How do I login?
As you explore Leber congenital amaurosis - Global Genes web sites you may encounter content that is only accessible to Leber congenital amaurosis - Global Genes Members and registered visitors. Should you encounter this type of content, a login screen displays and you need to create an account. Upon completing the registration process you will be able to login using the email and password you entered during account creation. For return visits enter your Username and Password in the login box.

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