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Grover disease: review of subtypes with a focus on management options.
Aldana PC, Khachemoune A. Aldana PC, et al. Int J Dermatol. 2020 May;59(5):543-550. doi: 10.1111/ijd.14700. Epub 2019 Nov 14. Int J Dermatol. 2020. PMID: 31724740 Review.
In more severe cases that are refractory to less aggressive therapy, systemic corticosteroids, retinoids, and phototherapy may lead to successful resolution. Novel therapies are few and have little evidence but involve innovative use of light therapy and immu …
In more severe cases that are refractory to less aggressive therapy, systemic corticosteroids, retinoids, and phototherapy may lead t …
Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotype.
Arin MJ, Grimberg G, Schumann H, De Almeida H Jr, Chang YR, Tadini G, Kohlhase J, Krieg T, Bruckner-Tuderman L, Has C. Arin MJ, et al. Br J Dermatol. 2010 Jun;162(6):1365-9. doi: 10.1111/j.1365-2133.2010.09657.x. Epub 2010 Feb 25. Br J Dermatol. 2010. PMID: 20199538
We identified for the first time a patient with compound heterozygosity for KRT5 mutations causing Dowling-Degos disease and EBS. CONCLUSIONS: Identification of novel mutations and genotype-phenotype correlations in EBS allow improved understanding of disease …
We identified for the first time a patient with compound heterozygosity for KRT5 mutations causing Dowling-Degos disease …