Epidermolysis Bullosa (EB) is an ultra-rare genetic disorder characterized by fragility of the eyes and skin, making them prone to blistering and tearing from minor friction or trauma. This condition primarily affects children, presenting a lifelong challenge that demands specialized care and attention.​​

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The ocular manifestations of this condition are profound and painful, and if left unaddressed, they can lead to blindness. Recognizing the pivotal role of ocular health in patient quality of life, we're driven to forge solutions that address this unmet need.