Confirmation of the role of a KRT5 mutation and successful management of skin lesions in a patient with Galli–Galli disease
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DOI: 10.1111/ced.13683
Abstract: Galli–Galli disease (GGD) is a rare autosomal dominant genodermatosis, which is considered an acantholytic variant of Dowling–Degos disease (DDD). It is characterized by reticular, lentigo-like hyperpigmentation on the groins, axillae and large folds, occurring between… read more here.
Keywords: krt5; krt5 mutation; dermatology; galli ... See more keywords