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A case of reticulate pigmented anomaly of the flexures (Dowling-Degos disease)

Title
A case of reticulate pigmented anomaly of the flexures (Dowling-Degos disease)
Authors
Jeon H.J.Kim S.H.Whang K.K.Hahm J.H.
Ewha Authors
함정희황규광
Issue Date
2006
Journal Title
Korean Journal of Dermatology
ISSN
0494-4739JCR Link
Citation
Korean Journal of Dermatology vol. 44, no. 7, pp. 877 - 880
Indexed
SCOPUS; KCI scopus
Document Type
Article
Abstract
Dowling-Degos disease is a rare autosomal dominant genodermatosis with a genetically determined disturbance of epidermal proliferation. The clinical symptoms of Dowling-Degos disease are characterized by the acquired reticulate pigmented anomaly of the flexures. We report a case of Dowling-Degos disease in a 27-year-old female, who presented with numerous small, hyperpigmented macules in reticular pattern, localized to the axillae, inframammary and inguinal areas, popliteal fossa, neck, and face.
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의과대학 > 의학과 > Journal papers
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