Results 151 to 160 of about 7,515 (243)

Desmoplakin mutation underlying autosomal dominant arrhythmogenic cardiomyopathy, palmoplantar keratoderma, and curly hair. [PDF]

open access: yesJAAD Case Rep, 2023
Kincaid C   +5 more
europepmc   +1 more source

Palmoplantar Keratoderma and Nail Involvement in an Adult.

open access: yesIndian J Dermatol, 2023
Sethia K, Arora P, Sachdeva S.
europepmc   +1 more source

Striate palmoplantar keratoderma of Brünauer-Fuhs-Siemens

open access: diamond, 2021
Sandra Valenzuela‐­Ubiña   +2 more
openalex   +1 more source

Case Report: Autosomal recessive palmoplantar keratoderma with additional bilateral hearing loss due to a pathogenic frameshift deletion in <i>FAM83G</i>. [PDF]

open access: yesFront Med (Lausanne)
Mora-Gómez M   +16 more
europepmc   +1 more source

Palmoplantar keratoderma: An unusual manifestation of hypohydrotic ectodermic dysplasia. [PDF]

open access: yesClin Case Rep, 2022
Abdelli W   +6 more
europepmc   +1 more source

Autosomal dominant SLURP1 variants cause palmoplantar keratoderma and progressive symmetric erythrokeratoderma. [PDF]

open access: yesBr J Dermatol
Jiang X   +7 more
europepmc   +1 more source

DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma. [PDF]

open access: yesFront Cardiovasc Med, 2023
Heliö K   +10 more
europepmc   +1 more source

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