Guidance & Care

For patients, families, and friends, a diagnosis of Epidermolysis Bullosa carries with it great uncertainty.

All about Epidermolysis Bullosa (EB)

All about Epidermolysis Bullosa (EB)

See an overview of what EB is, how it’s inherited & how it’s diagnosed

Guidance & Care - products

Products

Information on exceptional products suitable for Epidermolysis Bullosa wounds & skin

Guidance & Care resources

Resources

All the essentials on wound care, caring for newborns, community tips & helpful organizations, & foundations

Contact the Epidermolysis Bullosa Team

Contact Options

Arrow icon
Call us at

855-532-5463

Arrow icon
Email us at

ebline@adapthealth.com

Arrow icon
Fax us at

877-651-1957

Order Epidermolysis Bullosa Supplies

Error message
Form submitted
Your form has been successfully submitted. AdaptHealth team will review it shortly and follow up with next steps.

Contact Options

Arrow icon
Call us at

855-532-5463

Arrow icon
Email us at

ebline@adapthealth.com

Arrow icon
Fax us at

877-651-1957

Order Epidermolysis Bullosa Supplies

Error message
Form submitted
Your form has been successfully submitted. AdaptHealth team will review it shortly and follow up with next steps.

What is EB?

EB (Epidermolysis Bullosa) is a genetic disorder causing fragility of the skin and sometimes other organs. Blisters and erosions form easily from minor trauma or even spontaneously, leading to pain and discomfort.

Causes

Blisters and erosions appear when the skin layers fail to adhere correctly. Normally, the epidermis (outer layer) is anchored to the dermis (deeper layer) by microscopic structures called fibrils and hemidesmosomes. When these don’t work properly, skin separates easily, leading to EB.

Types of EB

Plus Icon

EB Simplex (EBS):

Epidermis
Plus Icon

Junctional EB (JEB):

Dermal-epidermal junction
Plus Icon

Dystrophic EB (DEB):

Dermis
Plus Icon
Kindler Syndrome: Mixed type, affecting multiple skin layers

Diagnosis

Identifying the EB subtype can be challenging, especially in newborns and infants. Diagnosis often involves skin biopsy for electron microscopy and immunoepitope mapping, which helps pinpoint the affected skin layer and guides genetic testing.

Inheritance & Severity

EB types are classified by inheritance patterns (dominant or recessive) and their severity, based on blister localization and organ involvement. Severity varies depending on the genes involved and can include additional features such as nail changes or internal complications.

Genetic Testing

Specific EB subtypes are confirmed by genetic testing to identify mutations. In some cases, no mutation is found, but further testing may reveal involved genes. Knowing the mutation helps predict the severity and manage complications.

Research & Future

Ongoing genetic studies and clinical trials continue to expand knowledge of Epidermolysis Bullosa, supporting the search for new treatments and better patient outcomes.

Wound Care Products

There are thousands of exceptional wound care products available, and many are suitable for EB wounds and skin. This chart lists product categories and their properties.

Information on exceptional products suitable for Epidermolysis Bullosa wound care

Product Category

Absorption

Fight Infection

Non-Adherence

Protection

Retention

Alginate Dressings

Antimicrobial Dressings

Collagen Dressings

Contact Layer

Foam Dressings

Honey Dressings

Product Category

Absorption

Fight Infection

Non-Adherence

Protextion

Retention

Hydrogels

Impregnated Gauze Dressings

Keratin Products

Retention Dressings

Specialty Absorbent Dressings

Tape

ResMed Cleaning Tips
Respironics Cleaning Tips

Product Category

Absorption

Fight Infection

Non-Adherence

Protextion

Retention

Topicals, Ointments, & Creams

ResMed Cleaning Tips
Respironics Cleaning Tips

Helpful Resources

Contact us

Get in touch with the EB Team

Arrow icon
Call us at

855-532-5463

Arrow icon
Email us at

ebline@adapthealth.com

Arrow icon
Fax us at

877-651-1957