Results 111 to 120 of about 1,347 (192)

Type IV pityriasis rubra pilaris treated with ixekizumab. [PDF]

An Bras Dermatol
Ferreirinha A, João A, Brito Caldeira M.   +2 more
europepmc   +1 more source

Proteolytic dysregulation in the skin: insight from rare monogenic skin diseases. [PDF]

Cell Tissue Res
Li Z, Wang S, Blaydon DC, Kelsell DP.
europepmc   +1 more source

Diffuse palmoplantar keratoderma associated with acrocyanosis and livedo reticularis. Two sporadic cases.

Acta Dermato-Venereologica, 1995
N Ohtake, K Sou, K Tsukamoto, M Furue, K Tamaki   +4 more
openaire   +1 more source

Heterozygous pathogenic variants in <i>SERPINB7</i> potentially associated with Nagashima-type palmoplantar keratoderma and Hashimoto's thyroiditis: a case report. [PDF]

Open Life Sci
Liang H, Chen Y.
europepmc   +1 more source

A frameshift variation in the DSP gene causes a novel subtype of atypical epidermolytic palmoplantar keratoderma: Case report. [PDF]

Front Med (Lausanne)
Lin C, Chen H, Lai S, Huang S, Guo Z, Xie L, Zheng W, Lu J, Zeng Z, Wan C, Li L.   +10 more
europepmc   +1 more source

A case of Schopf-Schulz-Passarge syndrome

Schopf-Schulz-Passarge syndrome (SSPS) is a rare ectodermal dysplasia characterized by hypodontia, hypotrichosis, nail dystrophy, palmoplantar keratoderma, and periocular and eyelid margin apocrine hidrocystomas.
Hampton PJ, Angus B, Carmichael AJ
core  

A Case of Palmoplantar Keratodermas Complicated by Pseudoainhum and Literature Review. [PDF]

Clin Cosmet Investig Dermatol
Ye J, Li W, Yang X, Shi Y, Lv W.
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]

Front Med (Lausanne)
Mora-Gómez M, Feito M, Gallego-Zazo N, Maseda-Pedrero R, Sobral-Costas TG, Miranda-Alcaraz L, Vásquez-Amell V, Rodríguez-Canó M, Parra A, Cazalla M, Arias P, Silván C, Jiménez-Estrada JA, Ruiz-Pérez VL, Nevado J, Lapunzina P, Tenorio-Castano J.   +16 more
europepmc   +1 more source

A case report of palmoplantar keratoderma in a 3-year-old girl: A structured approach in primary care settings. [PDF]

Malays Fam Physician
Mohd Noor AA, Abdul Hadi A, Che Abdul Rahim AR.   +2 more
europepmc   +1 more source

A novel heterozygous missense mutation of the desmoglein 1 gene in a Chinese family with diffuse nonepidermolytic palmoplantar keratoderma

Indian Journal of Dermatology, Venereology and Leprology, 2018
Sheng Wang, Dan Wang, Yongping He
openaire   +1 more source