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Article

A case report of Dowling-Degos disease caused by POFUT1 exon deletion with possible coexistent CARD14 mutation-related psoriasis.

Journal of the European Academy of Dermatology and Venereology : JEADV - 1 Aug 2022

Liu Z, Zhu Z, Luo J, Yang B

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Share to CARD Signaling Adaptor Proteins
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 35340079
DOI: 10.1111/jdv.18105

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A case report of Dowling-Degos disease caused by POFUT1 exon deletion with possible coexistent CARD14 mutation-related psoriasis.PMID 35340079Read ↗

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A novel mutation in POFUT1 gene associated with Dowling-Degos disease and hidradenitis suppurativa.Semantic proximity Read ↗

Autosomal dominant familial generalized pustular psoriasis caused by a CARD14 mutation.Semantic proximity Read ↗

Analysis of POFUT1 gene mutation in a Chinese family with Dowling-Degos disease.Semantic proximity Read ↗

Novel POFUT1 mutation associated with hidradenitis suppurativa–Dowling–Degos disease firm up a role for Notch signalling in the pathogenesis of this disorderSemantic proximity Read ↗

Beneath the surface: delineating the subtypes of Dowling-Degos disease.Semantic proximity Read ↗

Dowling-Degos disease co-presenting with Darier disease.Semantic proximity Read ↗

Terbinafine-induced generalized pustular psoriasis in a patient carrying CARD14 mutation.Semantic proximity Read ↗

Mutations in POFUT1, Encoding Protein O-fucosyltransferase 1, Cause Generalized Dowling-Degos DiseaseSemantic proximity Read ↗

Dowling‐Degos disease: a reviewSemantic proximity Read ↗

A novel mutation in a CARD14-associated papulosquamous eruption.Semantic proximity Read ↗

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