Epidermolysis bullosa

Definition

Epidermolysis bullosa (EB) is a group of genetic skin diseases that cause the skin to blister very easily. Blisters form in response to minor injuries or friction, such as rubbing or scratching. There are four main types of epidermolysis bullosa: dystrophic epidermolysis bullosa Epidermolysis bullosa simplex Junctional epidermolysis bullosa Kindler Syndrome Identifying the exact type can be hard because there are many subtypes of EB. Within each type or subtype, a person may be mildly or severely affected. The disease can range from being a minor inconvenience to completely disabling, and fatal in some cases. Most types of EB are inherited. The inheritance pattern may be autosomal dominant or autosomal recessive. Management involves protecting the skin, reducing friction against the skin, and keeping the skin cool.

Also known as epidermolysis bullosa — per MONDO

Also identified as

• DOID 2730 per MONDO
• ICD10CM Q81 per MONDO
• ICD9 757.39 per MONDO
• MESH D004820 per MONDO
• NCIT C67383 per MONDO
• SCTID 61003004 per MONDO
• UMLS C0014527 per MONDO

Affected Organs