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Aquagenic keratoderma, also known as acquired aquagenic palmoplantar keratoderma, [4]: 788 transient reactive papulotranslucent acrokeratoderma, [4] aquagenic syringeal acrokeratoderma, [4] and aquagenic wrinkling of the palms, [2] is a skin condition characterized by the development of white papules on the palms after water exposure.
Punctate palmoplantar keratoderma. Keratosis punctata palmaris et plantaris; Spiny keratoderma; Focal acral hyperkeratosis; Complex keratodermas Diffuse palmoplantar keratoderma. Erythrokeratodermia variabilis; Palmoplantar keratoderma of Sybert; Olmsted syndrome; Naegeli–Franceschetti–Jadassohn syndrome; Focal palmoplantar keratoderma
Palmoplantar keratoderma cum degeneratione granulosa Vörner; Palmoplantar keratoderma of the Norrbotten type; Palmoplantar keratoderma striata; Palmoplantar keratoderma with knuckle pads and leukonychia and deafness; Palmoplantar keratoderma with periodontitis; Palmoplantar keratoderma with periodontitis and arachnodactyly and acro-osteolysis
PLS is characterized by periodontitis and palmoplantar keratoderma. [6] The severe destruction of periodontium results in loss of most primary teeth by the age of 4 and most permanent teeth by age 14. Hyperkeratosis of palms and soles of feet appear in first few years of life.
Keratoderma blennorrhagicum (from kerato- 'keratinized' derma- 'skin' blenno- 'mucous' and -rrhagia 'discharge'; also called keratoderma blennorrhagica) [1] are skin lesions commonly found on the palms and soles but which may spread to the scrotum, scalp and trunk. The lesions may resemble psoriasis. [2]: 195
Most of the signs of Haim–Munk syndrome begin to manifest during the first 2–4 years of life. [5] Commons signs at this stage are thickening and scaling of the skin of the palms, soles (palmoplantar keratoderma) and elbows, and shedding of the primary dentition caused by recurrent episodes of dental caries and periodontitis.
Acrokeratoelastoidosis of Costa or Acrokeratoelastoidosis is a hereditary form of marginal keratoderma, and can be defined as a palmoplantar keratoderma. It is distinguished by tiny, firm pearly or warty papules on the sides of the hands and, occasionally, the feet. It is less common than the hereditary type of marginal keratoderma ...
The hands and feet usually are the first to show signs of the disease but the disease can advance to other parts of the body. Signs of the disease include thickening of the skin, on hands and soles of feet, which can turn red in color. [6] There currently is no cure and treatment is limited, but Acitretin can be used in severe cases. [7]