Lack of TP53 mutations in a case of porokeratosis palmaris, plantaris et disseminata

S Ozkan; E Fetil; T Aydoğan; N Atabey; V Erkizan; U Pabuçcuoğlu; A T Güneş

doi:10.1159/000018462

Lack of TP53 mutations in a case of porokeratosis palmaris, plantaris et disseminata

Dermatology. 2000;201(2):158-61. doi: 10.1159/000018462.

Authors

S Ozkan¹, E Fetil, T Aydoğan, N Atabey, V Erkizan, U Pabuçcuoğlu, A T Güneş

Affiliation

¹ Department of Dermatology, Faculty of Medicine, University of Dokuz Eylül, Izmir, Turkey.

PMID: 11053922
DOI: 10.1159/000018462

Abstract

A 73-year-old man with porokeratosis palmaris, plantaris et disseminata is presented. He had punctate, guttate and annular hyperkeratotic papular lesions widespread on his body with thorn-like hyperkeratosis on the palms and soles. Lesional skin did not show mutations of TP53 exons 5-6, 7, 8.

Publication types

Case Reports

MeSH terms

Adolescent
Aged
DNA / genetics
Family Health
Humans
Male
Middle Aged
Mutation
Pedigree
Polymorphism, Single-Stranded Conformational
Porokeratosis / genetics
Porokeratosis / pathology*
Tumor Cells, Cultured
Tumor Suppressor Protein p53 / genetics*

Substances

Tumor Suppressor Protein p53
DNA