A Case of Family with Vörner-type Palmoplantar Keratoses Confirmed by Genetic Analysis

Author:

MATSUMOTO Kanae1,KANEKO Sakae1,TAKEUCHI So2,TAKEICHI Takuya2,AKIYAMA Masashi2

Affiliation:

1. Department of Dermatology, Masuda Red Cross Hospital

2. Department of Dermatology, Nagoya University school of medicine

Publisher

Western Japan Division of JDA

Subject

Dermatology

Reference15 articles.

1. 1) Thomas BR, O'Toole EA : Diagnosis and Management of Inherited Palmoplantar Keratodermas. Acta Derm Venereol, 2020 ; 100 : 168-176.

2. 2) Sakiyama T, Kubo A : Hereditary palmoplantar keratoderma "clinical and genetic differential diagnosis". J Dermatol, 2016 ; 43 : 264-274.

3. 3) Li Y, Tang L, Han Y et al : Genetic Analysis of KRT9 Gene Revealed Previously Known Mutations and Genotype-Phenotype Correlations in Epidermolytic Palmoplantar Keratoderma. Front Genet, 2019, doi : 10.3389/fgene. 2018.00645, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330350/pdf/fgene-09-00645.pdf, (2021-10-7).

4. 4) 野村和夫 : 掌蹠角化症-ケラチン分子異常を中心として. 医学のあゆみ, 2001 ; 199 : 697-700.

5. 5) Xiao H, Guo Y, Yi J et al : Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar Keratoderma. Cell Physiol Biochem, 2018 ; 46 : 1919-1929.

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