A very rare form of focal palmoplantar keratoderma with characteristics of painful circumscribed hyperkeratotic lesions on weight-bearing areas of soles, moderate focal hyperkeratosis of palmar pressure-related areas and an asymptomatic leukokeratosi

SNOMEDCT-BE (disorder) / 764963007

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kératodermie palmoplantaire ponctuée type 1

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A very rare hereditary skin disease with manifestation of irregularly distributed epidermal hyperkeratosis of the palms and soles. Reported in 35 families worldwide to date. The lesions usually start to develop in early adolescence but can also prese

SNOMEDCT-BE (disorder) / 717184007

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syndrome de dyskératose intraépithéliale cornéenne-kératodermie palmoplantaire-dyskératose laryngée

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Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome

SNOMEDCT-BE (disorder) / 773577009

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syndrome de kératodermie palmoplantaire diffuse-acrocyanose

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Syndrome with the association of diffuse palmoplantar keratoderma and acrocyanosis. It has been described in eight members of one family and in two sporadic cases. The mode of inheritance in the familial cases was autosomal dominant.

SNOMEDCT-BE (disorder) / 721096008

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kératodermie palmoplantaire ponctuée type 2

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Punctate palmoplantar keratoderma type 2

SNOMEDCT-BE (disorder) / 765096001

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kératodermie palmoplantaire type Nagashima

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Palmoplantar keratoderma Nagashima type