An autosomal-dominant form of macular dystrophy in which central, non-correctable, and progressive visual loss begins in childhood or adolescence and worsens in adulthood. The disease is characterized by degeneration of the pigment epithelium of the macula.
Encounter a genetic disorder characterized by an abnormality in the macula, a crucial part of the light-sensitive retina located at the back of the eye. This congenital condition manifests from birth and leads to the gradual deterioration of vision over time. The progressive loss of vision associated with this disorder underscores the importance of the macula in visual function and clarity. Understanding the nature of this genetic condition aids in early diagnosis and management, ensuring appropriate support and interventions are provided to individuals affected by this disorder.