Galli-Galli Disease: A Rare Acantholytic Variant of Dowling-Degos Disease

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Galli-Galli Disease: A Rare Acantholytic Variant of Dowling-Degos Disease

Galli-Galli disease is a rare acantholytic variant of Dowling-Degos disease, with few cases reported in the literature. We describe a case of Galli-Galli disease and review the literature.

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Galli-Galli disease is an acantholytic variant of Dowling-Degos disease: additional genetic evidence in a German family.

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Mutations in POGLUT1 in Galli–Galli/Dowling–Degos disease

DEAR EDITOR, The group of reticulate pigmentary disorders includes the rare autosomal dominant Dowling–Degos disease (DDD) and Galli–Galli disease (GGD; OMIM 179850, 615327 and 615696). 1 In light of substantial clinical, histological and mutational overlap between GGD and DDD, they are considered to belong to the same entity. 2,3 Mutations in KRT5 (encoding keratin 5) have been associated with...

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Dowling Degos disease is characterised by hyperpigmented macules arranged in a reticulate pattern in the flexures. The rare hypopigmented variant shows characteristic acanthosis with antler like rete ridges but with pigment only at the tips of the rete ridges. We describe here a rare variant with coexistence of characteristic reticulate hyperpigmentation and hypopigmented macules, which has bee...

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[Galli-Galli disease presenting as lichenoid papules in the flexures].

Galli-Galli disease is a rare genodermatosis currently regarded as an acantholytic variant of Dowling-Degos disease. The 2 diseases have the same clinical features: reticular hyperpigmented macules in the great skin folds, erythematous scaly papules and plaques, comedo-like lesions, and pitted perioral scars, and the only differentiating characteristic is the histological finding of acantholysi...

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ژورنال

عنوان ژورنال: Case Reports in Medicine

سال: 2011

ISSN: 1687-9627,1687-9635

DOI: 10.1155/2011/703257