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A Case of Reticulate Pigmented Anomaly of the Flexures (Dowling-Degos Disease) / 대한피부과학회지
Korean Journal of Dermatology ; : 877-880, 2006.
Article in Korean | WPRIM | ID: wpr-24214
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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Full text: Available Index: WPRIM (Western Pacific) Main subject: Axilla / Neck Limits: Adult / Female / Humans Language: Korean Journal: Korean Journal of Dermatology Year: 2006 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Axilla / Neck Limits: Adult / Female / Humans Language: Korean Journal: Korean Journal of Dermatology Year: 2006 Type: Article