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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Acrochordons Anomalies des dermatoglyphes Cutis laxa (hyperelastica) Kératose:folliculaire [Darier-White] | palmoplantaire héréditaire | Pemphigus bénin familial [Hailey-Hailey] Plis palmaires anormaux

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Abnormal palmar creases Accessory skin tags Benign familial pemphigus [Hailey-Hailey] Cutis laxa (hyperelastica) Dermatoglyphic anomalies Inherited keratosis palmaris et plantaris Keratosis follicularis [Darier-White]

WORLD HEALTH ORGANIZATION ICD-10: Q82.8

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kératodermie palmoplantaire focale et gingivale

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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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porokératose palmoplantaire et disséminée

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A rare form of porokeratosis occurring mainly in adolescence and characterised by small pruritic or painful keratotic papules that first appear on the palms and soles, and may gradually become generalised. The prevalence is unknown but it is one of t

SNOMEDCT-BE (disorder) / 718218005

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Others have searched : darier-white hailey-hailey pemphigus bénin familial plis palmaires anormaux kératodermie palmoplantaire focale et gingivale kératodermie palmoplantaire ponctuée type kératome palmoplantaire kératose palmoplantaire diffuse palmoplantaire héréditaire porokératose palmoplantaire et disséminée syndrome main-pied érythrodysesthésie palmoplantaire

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érythrodysesthésie palmoplantaire

Date index:2023-02-26 -

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Translation of "érythrodysesthésie palmoplantaire " (French → English) :

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