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  2. Palmoplantar keratoderma - Wikipedia

    en.wikipedia.org/wiki/Palmoplantar_keratoderma

    Palmoplantar keratodermas are a heterogeneous group of skin disorders characterized by abnormal thickening (scleroderma) of the stratum corneum of the palms and soles. Autosomal recessive, dominant, X-linked, and acquired forms have all been described in medical literature. [1]: 505 [2]: 211 [3]

  3. Meleda disease - Wikipedia

    en.wikipedia.org/wiki/Meleda_disease

    Quality of life can possibly can be decreased, therefore getting treatment is recommended. [6] Too much dry skin can be painful for some and cause discomfort. [ 8 ] There is limited data on the life expectancy of an affected person, but this disease alone does not reduce a person's lifespan.

  4. Acrokeratoelastoidosis of Costa - Wikipedia

    en.wikipedia.org/wiki/Acrokeratoelastoidosis_of...

    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.

  5. Papillon–Lefèvre syndrome - Wikipedia

    en.wikipedia.org/wiki/Papillon–Lefèvre_syndrome

    Papillon–Lefèvre syndrome (PLS), also known as palmoplantar keratoderma with periodontitis, [1] [2] is an autosomal recessive [3] genetic disorder caused by a deficiency in cathepsin C. [ 4 ] [ 5 ]

  6. Keratoderma - Wikipedia

    en.wikipedia.org/wiki/Keratoderma

    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

  7. Haim–Munk syndrome - Wikipedia

    en.wikipedia.org/wiki/Haim–Munk_syndrome

    Haim–Munk syndrome (also known as "palmoplantar keratoderma with periodontitis and arachnodactyly, acro-osteolysis and Cochin Jewish syndrome" [1]) is a skin disease caused, like Papillon–Lefèvre syndrome, by a mutation in the cathepsin C gene. [1] One of its features is thick curved finger and toenails. [2]

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