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Article

Clinical and molecular dilemmas in the diagnosis of familial epidermolysis bullosa pruriginosa.

Journal of the American Academy of Dermatology - 1 May 2007

Ee Hock Leong, Liu Lu, Goh Chee Leok, McGrath John A

Abstract excerpt

Dystrophic epidermolysis bullosa is a rare and clinically heterogeneous mechanobullous disorder. One unusual clinical variant is epidermolysis bullosa pruriginosa (EBP), in which the combination of pruritus and skin fragility can lead to hypertrophic, lichenified nodules and plaques. This form of inherited epidermolysis bullosa may not develop clinically until adult life, leading to diagnostic confusion with...

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Source

Identifiers

PMID: 17434045
DOI: 10.1016/j.jaad.2006.10.017

Genes

EBP

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Clinical and molecular dilemmas in the diagnosis of familial epidermolysis bullosa pruriginosa.PMID 17434045Read ↗

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