Dystrophic epidermolysis bullosa (Q46639): Difference between revisions

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+CID11:EC32
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+dki-india-EC32
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+Concluído
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+https://pauloleads.com.br/cases-publicos/
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+August 2026Timestamp +2026-08-13T00:00:00Z
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Calendar Gregorian
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@@ Property / Collection date: 13 August 2026 / rank @@
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+CLINICA CR FERNANDES
@@ Property / Linked ICD 10: CLINICA CR FERNANDES / rank @@
+Normal rank

Latest revision as of 15:21, 13 August 2026

Dystrophic (dermolytic) epidermolysis bullosa is due to defects in or absence of type VII collagen. As a result the anchoring fibrils which secure the epidermal basement membrane to the dermis are defective or absent. The severe recessive form causes extensive scarring and predisposes to aggressive squamous cell carcinoma.

Language	Label	Description	Also known as
default for all languages	EC32
English	Dystrophic epidermolysis bullosa	Dystrophic (dermolytic) epidermolysis bullosa is due to defects in or absence of type VII collagen. As a result the anchoring fibrils which secure the epidermal basement membrane to the dermis are defective or absent. The severe recessive form causes extensive scarring and predisposes to aggressive squamous cell carcinoma.