There are 3 main types of EB. They are:

• Dystrophic epidermolysis bullosa
• Epidermolysis bullosa simplex
• Junctional epidermolysis bullosa

EB can vary in severity from minor to fatal. The minor forms cause blistering of the skin. The fatal forms affect other organs. Most types of this condition start at birth or soon after. It can be hard to identify the exact type of EB a person has, although specific genetic markers are now available for most.

Family history is a risk factor. The risk is higher if a parent has this condition.

Another rare type of EB is called epidermolysis bullosa acquisita. This form develops after birth. It is an autoimmune disorder, which means the body attacks itself.

Depending on the form of EB, symptoms can include:

• Alopecia (hair loss)
• Blisters around the eyes and nose
• Blisters in or around the mouth and throat, causing feeding problems or swallowing difficulty
• Blisters on the skin as a result of minor injury or temperature change, especially of the feet
• Blistering that is present at birth
• Dental problems, such as tooth decay
• Hoarse cry, cough, or other breathing problems
• Tiny white bumps on previously injured skin
• Nail loss or deformed nails
• Mitten-like hands or feet
• Thickening of skin on hands and feet
• Muscle, heart, brain, gastrointestinal, bone, or kidney issues

Your health care provider will look at your skin to diagnose EB.

Tests that are used to confirm the diagnosis include:

• Genetic testing
• Skin biopsy
• Special tests of skin samples under a microscope

Skin tests may be used to identify the form of EB.

Other tests that may be done include:

• Blood test for anemia
• Culture to check for bacterial infection if wounds are healing poorly
• Imaging studies to look at other organs

The growth rate will be checked often for a baby who has or may have EB.

The goal of treatment is to prevent blisters from forming and avoiding complications. Other treatment will depend on how bad the condition is.

HOME CARE

Follow these guidelines at home:

• Take good care of your skin to prevent infections.
• Follow your provider's advice if blistered areas become crusted or raw. You might need regular whirlpool therapy and to apply antibiotic ointments to wound-like areas. Your provider will let you know if you need a bandage or a dressing, and if so, what type to use.
• You may need to use oral steroid medicines for short periods of time if you have swallowing problems. You may also need to take medicine if you get a candida (yeast) infection in the mouth or throat.
• Take good care of your oral health and get regular dental check-ups. It is best to see a dentist who has experience treating people with EB.
• Eat a healthy diet. When you have a lot of skin injury, you may need extra calories and protein to help your skin heal. Choose soft foods and avoid nuts, chips, and other crunchy foods if you have sores in your mouth. A nutritionist can help you with your diet.
• Do exercises a physical therapist shows you to help keep your joints and muscles mobile.

SURGERY

Surgery to treat this condition may include:

• Skin grafting in places where sores are deep
• Dilation (widening) of the esophagus if there is a narrowing
• Repair of hand deformities
• Removal of any squamous cell carcinoma (a type of skin cancer) that develops

OTHER TREATMENTS

Other treatments for this condition may include:

• Medicines that suppress the immune system may be used for the autoimmune form of this condition.
• Protein and gene therapy and the use of the medicine interferon are being studied.

The outlook depends on the severity of the illness.

Infection of the blistered areas is common.

Mild forms of EB improve with age. Very serious forms of EB have a very high death rate.

In the severe forms, scarring after blisters form may cause:

• Contracture deformities (for example, at the fingers, elbows, and knees) and other deformities
• Swallowing problems if the mouth and esophagus are affected
• Fused fingers and toes
• Limited mobility from scarring

These complications may occur:

• Anemia
• Reduced life span due to severe forms of the condition
• Esophageal narrowing
• Eye problems, including blindness
• Infection, including sepsis (infection in the blood)
• Loss of function in the hands and feet
• Muscular dystrophy
• Periodontal disease
• Cardiac problems
• Kidney failure
• Severe malnutrition caused by feeding difficulty, leading to failure to thrive
• Squamous cell skin cancer

If your infant has any blistering shortly after birth, contact your provider. If you have a family history of EB and plan to have children, you may want to have genetic counseling.

Genetic counseling is recommended for prospective parents who have a family history of any form of EB.

During pregnancy, a test called chorionic villus sampling may be used to test the baby. For couples at high risk of having a child with EB, the test can be done as early as week 8 to 10 of pregnancy. Talk to your provider.

To prevent skin damage and blistering, wear padding around injury-prone areas such as the elbows, knees, ankles, and buttocks. Avoid contact sports.

If you have EB acquisita and are on steroids for longer than 1 month, you may need calcium and vitamin D supplements. These supplements may help prevent osteoporosis (thinning bones).

EB; Junctional epidermolysis bullosa; Dystrophic epidermolysis bullosa; Hemidesmosomal epidermolysis bullosa; Weber-Cockayne syndrome; Epidermolysis bullosa simplex

Dinulos JGH. Vesicular and bullous diseases. In: Dinulos JGH, ed. Habif's Clinical Dermatology. 7th ed. Philadelphia, PA: Elsevier; 2021:chap 16.

Ferri FF. Epidermolysis bullosa. In: Ferri FF, ed. Ferri's Clinical Advisor 2025. Philadelphia, PA: Elsevier; 2025:434e15-434e17.

Fine J-D, Mellerio JE. Epidermolysis bullosa. In: Bolognia JL, Schaffer JV, Cerroni L, eds. Dermatology. 5th ed. Philadelphia, PA: Elsevier Limited; 2025:chap 32.

Updated by: Elika Hoss, MD, Assistant Professor of Dermatology, Mayo Clinic, Scottsdale, AZ. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.