Dowling-Degos disease (Q93301): Difference between revisions

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Latest revision as of 08:24, 16 August 2026

Dowling-Degos disease is a rare autosomal dominant condition which usually presents post-pubertally with multiple small, round pigmented freckle-like macules. They become progressively more numerous and may become reticulate with time. The axillae and groins are the usual sites, although other areas may be involved, including the intergluteal and inframammary folds, neck, scalp, trunk, arms and genitalia. Pigmentation is symmetrical and progressive, but is otherwise asymptomatic.

Language	Label	Description	Also known as
default for all languages	ID_15123132
English	Dowling-Degos disease	Dowling-Degos disease is a rare autosomal dominant condition which usually presents post-pubertally with multiple small, round pigmented freckle-like macules. They become progressively more numerous and may become reticulate with time. The axillae and groins are the usual sites, although other areas may be involved, including the intergluteal and inframammary folds, neck, scalp, trunk, arms and genitalia. Pigmentation is symmetrical and progressive, but is otherwise asymptomatic.