Epidermolysis Bullosa Dystrophica

Overview

Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. All forms of dystrophic epidermolysis bullosa result from mutations in COLLAGEN TYPE VII, a major component fibrils of BASEMENT MEMBRANE and EPIDERMIS.

This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.

Quick facts about Epidermolysis Bullosa Dystrophica

Topic type

Condition

Category

Dermatology

MeSH classification

C16.131.831.493.160|C16.320.850.275.160|C17.300.200.367|C17.800.804.493.160|C17.800.827.275.160|C17.800.865.410.160

Preparing for an appointment about Epidermolysis Bullosa Dystrophica

If you are speaking with a healthcare professional about Epidermolysis Bullosa Dystrophica, it can help to prepare a few details in advance.

• Write down your symptoms and when they started.
• Bring details of any medicines, supplements or previous treatments.
• Ask what tests or assessments may be needed.
• Ask what treatment or management options may be suitable.
• Ask when you should seek urgent medical help or follow-up care.

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