Epidermolysis bullosa (EB) is a rare genetic disorder that causes fragile skin

Leading to blisters and sores from minor friction or trauma. It can affect any part of the body, and its severity varies widely. There are different types of EB, each with distinct characteristics and genetic causes.

Here are some key points about EB:

1. Types: The main types include EB simplex, junctional EB, and dystrophic EB, each affecting different layers of the skin.

2. Symptoms: Common symptoms include blistering, sensitivity to touch, and skin peeling. Some forms also affect internal organs and can lead to complications.

3. Causes: EB is caused by mutations in genes responsible for producing proteins that help anchor the skin layers together.

4. Management: There is no cure for EB, but treatment focuses on wound care, pain management, and preventing infections. Supportive therapies and counseling can also help improve quality of life.

5. Awareness: Raising awareness about EB is crucial for fostering understanding and support for those affected. Advocacy groups work to provide resources, support, and research funding.

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