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.
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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