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Case Reports
. 2019 Dec;181(6):1312-1314.
doi: 10.1111/bjd.18221. Epub 2019 Aug 22.

Mast cell activation in Dowling-Degos disease

Affiliations
Case Reports

Mast cell activation in Dowling-Degos disease

J Knuever et al. Br J Dermatol. 2019 Dec.
No abstract available

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References

    1. Wu YH, Lin YC. Generalized Dowling-Degos disease. J Am Acad Dermatol 2007; 57:327-34.
    1. Betz RC. A path through the reticulate pigmentation disorder jungle. Br J Dermatol 2017; 177:893-4.
    1. Basmanav FB, Oprisoreanu AM, Pasternack SM et al. Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease. Am J Hum Genet 2014; 94:135-43.
    1. Basmanav FB, Fritz G, Lestringant GG et al. Pathogenicity of POFUT1 in Dowling-Degos disease: additional mutations and clinical overlap with reticulate acropigmentation of kitamura. J Invest Dermatol 2015; 135:615-8.
    1. Ralser DJ, Basmanav FB, Tafazzoli A et al. Mutations in γ-secretase subunit-encoding PSENEN underlie Dowling-Degos disease associated with acne inversa. J Clin Invest 2017; 127:1485-90.

MeSH terms

Supplementary concepts