Galli–Galli disease

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]

References

^ 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.

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[Andrews-1] James, William; Berger, Timothy; Elston, Dirk Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.

[2] Journal of the American Academy of Dermatology ISSN 0190-9622 CODEN JAADDB

[Bolognia-3] Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.

[1]

[2]

[3]

See also

References