Recessive dystrophic epidermolysis bullosa, generalised severe (Q96101): Difference between revisions
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15 August 2026
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Latest 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.
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| 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. |
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CID11:ID_365362994
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dki-india-ID_365362994
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Concluído
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15 August 2026
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