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Keratolysis exfoliativa (also known as" lamellar dyshidrosis ", [1] " recurrent focal palmar peeling ", [2] " recurrent palmar peeling " [1]: 212 [2]) is a sometimes harmless, sometimes painful skin condition that can affect the focal surface of the fingers and/or the palm or soles of the feet. It is often misdiagnosed as chronic contact ...
Dyshidrosis is a type of dermatitis, characterized by itchy vesicles of 1–2 mm in size, on the palms of the hands, sides of fingers, or bottoms of the feet. [8] Outbreaks usually conclude within three to four weeks, but often recur. [4][8] Repeated attacks may result in fissures and skin thickening. [7] The cause of the condition is not known.
Peeling skin syndrome 5 is caused by a genetic defect in the serpin (serpin family member 8) gene. This gene is produced by platelets and can bind to and inhibit the function of furin, which is a serine protease involved in platelet functions. It is also characterized by superficial peeling of the dorsal and palmar pores and skin of the hands ...
Erythrodermic psoriasis is serious and may be life-threatening. It causes redness and swelling in the skin that looks like a burn. This type of psoriasis covers at least 75% of the body ...
Psoriasis is a long-lasting, noncontagious autoimmune disease characterized by patches of abnormal skin. [ 4 ][ 5 ] These areas are red, pink, or purple, dry, itchy, and scaly. [ 8 ][ 3 ] Psoriasis varies in severity from small localized patches to complete body coverage. [ 3 ] Injury to the skin can trigger psoriatic skin changes at that spot ...
Scleroderma is a group of autoimmune diseases that may result in changes to the skin, blood vessels, muscles, and internal organs. [2][6][8] The disease can be either localized to the skin or involve other organs, as well. [2] Symptoms may include areas of thickened skin, stiffness, feeling tired, and poor blood flow to the fingers or toes with ...
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. Mild forms of the disease are the most common, consisting of skin rashes that flare up under ...
Keratolytic Winter erythema (also known as Oudtshoorn disease [1] or Oudtshoorn skin [2] [3]) is a rare autosomal dominant skin disease of unknown cause which causes redness and peeling of the skin on the palms and soles. [4] Onset, increased prominence and severity usually occurs during winter. [5] [6] It is a type of genodermatosis.