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Quoted phrase not found in phrase index: "Dowling-Degos disease 4"
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Dowling-Degos Disease in the Anogenital Region.
Belamarić M, Ljubojević Hadžavdić S. Belamarić M, et al. Acta Dermatovenerol Croat. 2022 Dec;30(4):261-262. Acta Dermatovenerol Croat. 2022. PMID: 36919394
Dowling-Degos disease (DDD) is a benign, rare genodermatosis (reticulate pigmented anomaly) of flexure sites with autosomal dominant inheritance (1,2).The disease is caused by a loss-of-function mutation of keratin 5 (KRT5) present on the chromosome 12q gene …
Dowling-Degos disease (DDD) is a benign, rare genodermatosis (reticulate pigmented anomaly) of flexure sites with autos …
Full ablative versus fractional ablative laser therapy for Dowling-Degos disease.
Seitz AT, Sterz H, Strehlow V, Nagel S, Dumann K, Grunewald S, Simon JC, Kunz M. Seitz AT, et al. Lasers Surg Med. 2019 Apr;51(4):321-324. doi: 10.1002/lsm.23021. Epub 2018 Oct 3. Lasers Surg Med. 2019. PMID: 30281812
Dowling-Degos disease (DDD) is a rare autosomal-dominant genodermatosis with limited treatment possibilities. ...After the three treatments were performed, the right side of the patient's upper abdomen and portions of her lower abdomen and chest were also tre …
Dowling-Degos disease (DDD) is a rare autosomal-dominant genodermatosis with limited treatment possibilities. ...After …
Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease.
Betz RC, Planko L, Eigelshoven S, Hanneken S, Pasternack SM, Bussow H, Van Den Bogaert K, Wenzel J, Braun-Falco M, Rutten A, Rogers MA, Ruzicka T, Nöthen MM, Magin TM, Kruse R. Betz RC, et al. Am J Hum Genet. 2006 Mar;78(3):510-9. doi: 10.1086/500850. Epub 2006 Jan 19. Am J Hum Genet. 2006. PMID: 16465624 Free PMC article.
Dowling-Degos disease (DDD) is an autosomal dominant genodermatosis characterized by progressive and disfiguring reticulate hyperpigmentation of the flexures. We performed a genomewide linkage analysis of two German families and mapped DDD to chromosome 12q, …
Dowling-Degos disease (DDD) is an autosomal dominant genodermatosis characterized by progressive and disfiguring reticu …
Co-existence of leukoderma with features of Dowling-Degos disease: reticulate acropigmentation of Kitamura spectrum in five unrelated patients.
Lestringant GG, Masouyé I, Frossard PM, Adeghate E, Galadari IH. Lestringant GG, et al. Dermatology. 1997;195(4):337-43. doi: 10.1159/000245984. Dermatology. 1997. PMID: 9529553
BACKGROUND: The spectrum of Dowling-Degos disease-reticulate acropigmentation of Kitamura (DDD-RAK) is a group of rare autosomal dominant disorders that have in common a unique histological picture of hyperpigmented digitate epidermal 'downgrowths'. Patients …
BACKGROUND: The spectrum of Dowling-Degos disease-reticulate acropigmentation of Kitamura (DDD-RAK) is a group of rare …
Galli-Galli Disease Presenting as a Lentigo-like Eruption: A Further Clinical Feature in the Wide Spectrum of Reticulate Pigment Disorders.
Paolino G, Donati M, Didona D, Panetta C, Donati P. Paolino G, et al. Acta Dermatovenerol Croat. 2017 Dec;25(4):300-302. Acta Dermatovenerol Croat. 2017. PMID: 30064605
Different clinical features can be present, including a reticular pattern and a freckle-like pattern with hyper- or hypo-pigmented macules (1). Dowling-Degos disease (DDD), an autosomal dominant genodermatosis, is the main type of RPD (2). ...These aspects co …
Different clinical features can be present, including a reticular pattern and a freckle-like pattern with hyper- or hypo-pigmented macules ( …