Biederman's Congenital Amaurosis is a rare genetic eye disorder that affects vision from birth. It is characterized by severe vision impairment or blindness due to abnormalities in the retina, particularly affecting the photoreceptor cells. Individuals with this condition may also experience other symptoms, such as nystagmus (involuntary eye movements) and sensitivity to light. The condition is caused by mutations in various genes, which can be inherited in different ways. Diagnosis typically involves a comprehensive eye examination and genetic testing. While there is currently no cure, early intervention and supportive therapies can help improve quality of life for those affected.