Galli–Galli disease
   HOME

TheInfoList



OR:

Galli–Galli disease is a rare inherited condition that has close resemblance clinically to Dowling-Degos' disease, but is histologically distinct, characterized by skin lesions that are 1- to 2-mm slightly keratotic red to dark brown papules which are focally confluent in a reticulate pattern.James, William; Berger, Timothy; Elston, Dirk ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. . The disease is also characterized by slowly progressive and disfiguring reticulate hyperpigmentation of the flexures, clinically and histopathologically diagnostic for Dowling-Degos disease but also associated with suprabasal, nondyskeratotic acantholysis.Journal of the American Academy of Dermatology ISSN 0190-9622 CODEN JAADDB


See also

*
List of cutaneous conditions Many skin conditions affect the human integumentary system—the organ system covering the entire surface of the body and composed of skin, hair, nails, and related muscle and glands. The major function of this system is as a barrier against t ...
* Skin lesion


References

Disturbances of human pigmentation {{Cutaneous-condition-stub