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Darier's disease (DD) is a rare, genetic skin disorder. It is an autosomal dominant disorder, that is, if one parent has DD, there is a 50% chance than a child will inherit DD. It was first reported by French dermatologist Ferdinand-Jean Darier in 1889.
It was first described by Darier in 1916. [ 3 ] [ 4 ] [ 5 ] Many different terms have been used to classify these types of lesions and it is still controversial on what exactly defines EAC. Some of the types include annular erythema (deep and superficial), erythema perstans, erythema gyratum perstans, erythema gyratum repens, darier erythema ...
Darier's sign is a change observed after stroking lesions on the skin of a person with systemic mastocytosis or urticaria pigmentosa. [1] In general, the skin becomes swollen, itchy and red. This is a result of compression of mast cells, which are hyperactive in these diseases. These mast cells release inflammatory granules which contain ...
Rosacea. What it looks like: Rosacea causes redness and thick skin on the face, usually clustered in the center.Easy flushing, a stinging sensation, and small, pus-filled pimples are other common ...
Polydactylous longitudinal erythronychia has been most commonly associated with Darier's disease [10] and lichen planus [11] but has also occasionally been associated with acantholytic epidermolysis bullosa, [12] no association, [13] graft-versus-host disease, [14] [15] hemiplegia, [16] and systemic amyloidosis. [11]
Acne symptoms and signs. Acne blemishes are most common on the face, chest, back, shoulders and neck, but they can appear almost anywhere. With acne, you might have pimples, blackheads, papules ...
Signs and symptoms of white lung pneumonia can vary based on what caused the illness in the first place, Dr. Ganjian says. However, these are the most common pneumonia symptoms, according to the ...
Darier's disease (Darier–White disease, dyskeratosis follicularis, keratosis follicularis) Linear Darier disease; DeSanctis–Cacchione syndrome; Disseminated superficial actinic porokeratosis; Disseminated superficial porokeratosis; Dolichol kinase deficiency; Dominant dystrophic epidermolysis bullosa; Dyskeratosis congenita (Zinsser–Cole ...