Recessive dystrophic epidermolysis bullosa, generalised severe (Q96101): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed label, description and/or aliases in pt-br, en
‎Changed an Item
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/365362994 / rank
 
Normal rank

Revision as of 11:58, 16 August 2026

Severe generalised recessive dystrophic epidermolysis bullosa is the most severe subtype of dystrophic epidermolysis bullosa. It was formerly known as the Hallopeau-Siemens type. It is characterised by generalised cutaneous and mucosal blistering and scarring associated with severe deformities and major extracutaneous involvement. Affected individuals are at high risk of aggressive squamous cell carcinomas in areas of chronic ulceration.
Language Label Description Also known as
default for all languages
ID_365362994
    English
    Recessive dystrophic epidermolysis bullosa, generalised severe
    Severe generalised recessive dystrophic epidermolysis bullosa is the most severe subtype of dystrophic epidermolysis bullosa. It was formerly known as the Hallopeau-Siemens type. It is characterised by generalised cutaneous and mucosal blistering and scarring associated with severe deformities and major extracutaneous involvement. Affected individuals are at high risk of aggressive squamous cell carcinomas in areas of chronic ulceration.

      Statements