Occurrence of multiple melanomas in a patient with punctate palmoplantar keratoderma type-1A associated to alpha and gamma adaptin binding protein [PDF]
Mirco Mastrangelo, PhD +7 more
doaj +5 more sources
Is punctate palmoplantar keratoderma type 1 associated with malignancy? A systematic review of the literature [PDF]
Background An association between punctate palmoplantar keratoderma type 1 (PPPK1) and malignancy has been proposed for decades. Some authors suggest that individuals with PPPK1 should undergo screening for various types of malignancies while others ...
S. B. Gram +5 more
doaj +2 more sources
Punctate Palmoplantar Keratoderma: A Case Report of Type 1 (Buschke-Fischer-Brauer Disease) [PDF]
Punctate palmoplantar keratoderma is a rare hereditary palmoplantar keratoderma. Herein we report a 59-year-old male, otherwise healthy, who presented with a 25-year history of asymptomatic persistent slowly progressing skin lesions on both hands.
Rahaf Bukhari +5 more
doaj +2 more sources
Unilateral Linear Punctate Palmoplantar Keratoderma: A Case Report [PDF]
Punctate palmoplantar keratoderma (PPPK) is a rare entity with an estimated prevalence rate of 1.17/100,000. PPPK usually presents with bilateral asymptomatic, tiny, hyperkeratotic punctate papules and plaques on the palmoplantar surface.
Chanisa Kiatsurayanon +5 more
doaj +2 more sources
New and recurrent AAGAB mutations in punctate palmoplantar keratoderma. [PDF]
Punctate palmoplantar keratoderma type I (PPPK1; also known as Buschke-Fischer-Brauer type; OMIM 148600) is an autosomal dominant disorder of keratinization, characterised by multiple hyperkeratotic lesions on palms and soles that usually start in early ...
Pohler E +9 more
europepmc +4 more sources
Multiple Yellowish and Keratotic Papules in the Thenar Eminence [PDF]
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Joana Calvão +3 more
doaj +3 more sources
Buschke–Fischer–Brauer Keratoderma: A Case Report of a Rare Skin Disorder [PDF]
Buschke–Fischer–Brauer keratoderma is a rare autosomal dominant disorder presenting as hyperkeratotic lesions on the palms and soles. Diagnosis requires clinical and histopathological evaluation. Management is symptomatic with keratolytics like salicylic
Dyala Sayed Ahmad +3 more
doaj +2 more sources
Clinical and Genetic Findings in Patients With Palmoplantar Keratoderma. [PDF]
IMPORTANCE: Palmoplantar keratoderma poses diagnostic challenges due to its clinical and genetic heterogeneity, and knowledge on the value of systematic genetic testing on clinically well-described patient cohorts is sparse.OBJECTIVE: To improve ...
Gram SB +10 more
europepmc +2 more sources
A case report of palmoplantar keratoderma in a 3-year-old girl: A structured approach in primary care settings. [PDF]
Palmoplantar keratoderma (PPK) is a dermatological disorder characterised by excessive thickening of the palms and soles, encompassing more than 20 conditions.
Mohd Noor AA +2 more
europepmc +3 more sources

