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 héréditaire type Gamborg-Nielsen

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Hereditary palmoplantar keratoderma Gamborg Nielsen type

SNOMEDCT-BE (disorder) / 717228004

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WORLD HEALTH ORGANIZATION ICD-10: D72.0

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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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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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kératodermie palmoplantaire striée ou en bandes

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Striate palmoplantar keratoderma

SNOMEDCT-BE (disorder) / 764958008

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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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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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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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Others have searched : darier-white hailey-hailey hypersegmentation hyposegmentation leucomélanopathie héréditaire may-hegglin pelger-huët pemphigus bénin familial plis palmaires anormaux kératodermie palmoplantaire focale et gingivale kératodermie palmoplantaire héréditaire kératodermie palmoplantaire héréditaire type gamborg-nielsen kératodermie palmoplantaire ponctuée type leucocytaire héréditaire palmoplantaire héréditaire porokératose palmoplantaire et disséminée syndrome de kératodermie palmoplantaire diffuse-acrocyanose

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palmoplantaire héréditaire

Date index:2024-05-05 -

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

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