2013
DOI: 10.7241/ourd.20134.145
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Eponyms in the dermatology literature linked to Palmo-Plantar Keratoderma

Abstract: Historical ArticlePalmoplantar keratodermas (PPKs) represent a diverse group of hereditary and acquired disorders characterized by hyperkeratosis of the skin on the palms and soles [1]. The three major patterns of involvement are diffuse, focal and punctate. There are clinical distinguishing features for each disease in this group, for example, transmigration to areas beyond the palmoplantar skin. Also the extent of associated systemic symptoms if present help in characterization of each type.Although a number… Show more

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Cited by 6 publications
(10 citation statements)
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“…Huriez syndrome [10] Palmoplantar keratoderma with scleroatrophy. Named for French dermatologist, Claude Huriez (1907-1984), ( Fig.…”
Section: Remarksmentioning
confidence: 99%
“…Huriez syndrome [10] Palmoplantar keratoderma with scleroatrophy. Named for French dermatologist, Claude Huriez (1907-1984), ( Fig.…”
Section: Remarksmentioning
confidence: 99%
“…Netherton syndrome (NS) [16] NS is characterized by the triad of trichorrhexis invaginata, ichthyosis linearis circumflexa, and an atopic diathesis. It is named after Earl Weldon Netherton, an American dermatologist.…”
Section: Hailey-hailey Disease [15]mentioning
confidence: 99%
“…Vohwinkel syndrome [6] Vohwinkel first described this autosomal dominant disorder in 1929. Honeycombed, diffuse hyperkeratosis of the palms and soles appears in infancy and then becomes transgredient.…”
mentioning
confidence: 99%
“…Jadassohn-Lewandowsky type of pachonychia congenital (PC) [6] This type 1 PC. Type 2 is known as Jackson-Lawler type.…”
mentioning
confidence: 99%
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