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Understanding Epidermolysis Bullosa (EB) | debra of America Epidermolysis Bullosa (EB) is a group of rare and complex genetic disorders that make the body’s largest organ, the skin, incredibly fragile Everyday activities—like walking, eating, or holding a pencil—can cause painful, recurrent blisters and widespread open wounds
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Epidermolysis Bullosa | Types, Symptoms, Diagnosis Treatment Epidermolysis Bullosa (EB) is a group of rare genetic conditions that affect one in every 50,000 children Epidermolysis Bullosa is hereditary, meaning that the genes that cause it may be are present in other family members
EB Disease - Patient Epidermolysis bullosa (EB) is a rare, inherited disease in which the skin is very fragile— so fragile that even just a friendly touch can injure it, leaving a painful blister or open wound
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