1989
DOI: 10.1016/0363-5023(89)90075-0
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Surgical treatment of epidermolytic hereditary palmoplantar keratoderma

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Cited by 6 publications
(1 citation statement)
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“…1 Described in 1924, PLS represents a constellation of disorders characterized by diffuse palmoplantar hyperkeratosis and rapidly progressing periodontitis of primary and permanent dentation, resulting from an autosomal recessive point mutation in the cathepsin C gene. Incidence ranges from 1 to 4 per million worldwide, with more than 300 cases reported.…”
Section: Dear Sirmentioning
confidence: 99%
“…1 Described in 1924, PLS represents a constellation of disorders characterized by diffuse palmoplantar hyperkeratosis and rapidly progressing periodontitis of primary and permanent dentation, resulting from an autosomal recessive point mutation in the cathepsin C gene. Incidence ranges from 1 to 4 per million worldwide, with more than 300 cases reported.…”
Section: Dear Sirmentioning
confidence: 99%