Results 131 to 140 of about 7,987 (210)

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

Bi-Allelic DSG1 Splice-Site Variant Identified in a Family With Non-Syndromic Striate Palmoplantar Keratoderma. [PDF]

open access: yesJ Dermatol
Ahmed S   +10 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

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 with dental abnormalities

open access: yesIndian Dermatology Online Journal, 2014
Feroze Kaliyadan, Ajit Nambiar
openaire   +3 more sources

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

Nagashima-type palmoplantar keratoderma

open access: yesIndian Journal of Dermatology, Venereology and Leprology
Tai-Li, Chen, Cheng-Yuan, Li
openaire   +2 more sources

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