Galli–Galli disease
| Galli–Galli disease | |
|---|---|
 | |
| This condition is inherited in an autosomal dominant manner. | |
| Specialty | Dermatology |
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.[1]: 856 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.[2][3]
See also
[edit]References
[edit]- ^ James, William; Berger, Timothy; Elston, Dirk Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
- ^ Journal of the American Academy of Dermatology ISSN 0190-9622 CODEN JAADDB
- ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
 | This cutaneous condition article is a stub. You can help Wikipedia by expanding it. |