Junctional epidermolysis bullosa inversa (Q103890): Difference between revisions

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16 August 2026
Timestamp+2026-08-16T00:00:00Z
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CalendarGregorian
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Latest revision as of 09:40, 17 August 2026

Junctional epidermolysis bullosa inversa is a rare severe subtype of junctional epidermolysis bullosa, characterised by blistering and erosions confined to intertriginous skin sites, the oesophagus, and vagina.
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ID_1191822552
    English
    Junctional epidermolysis bullosa inversa
    Junctional epidermolysis bullosa inversa is a rare severe subtype of junctional epidermolysis bullosa, characterised by blistering and erosions confined to intertriginous skin sites, the oesophagus, and vagina.

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      CID11:ID_1191822552
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      dki-india-ID_1191822552
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      Concluído
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      16 August 2026
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