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A case of reticulate pigmented anomaly of the flexures (Dowling-Degos disease)
- A case of reticulate pigmented anomaly of the flexures (Dowling-Degos disease)
- Jeon H.J.; Kim S.H.; Whang K.K.; Hahm J.H.
- Ewha Authors
- 함정희; 황규광
- Issue Date
- Journal Title
- Korean Journal of Dermatology
- Korean Journal of Dermatology vol. 44, no. 7, pp. 877 - 880
- SCOPUS; KCI
- Document Type
- 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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