Palmoplantar keratoderma with deafness due to GJB2 mutation can develop ichthyosiform symptoms: a case report

J Eur Acad Dermatol Venereol. 2022 Sep;36(9):e693-e695. doi: 10.1111/jdv.18135. Epub 2022 Apr 27.

Authors

A Kimura¹, T Miyauchi¹, J T Peh¹, T Yanagi¹, S Hasegawa², S Morita³, H Ujiie¹

Affiliations

¹ Department of Dermatology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
² Higashikariki Dermatology Clinic, Sapporo, Japan.
³ Department of Otolaryngology-Head & Neck Surgery, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

PMID: 35398937
DOI: 10.1111/jdv.18135

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Connexins / genetics
Deafness* / complications
Deafness* / genetics
Hearing Loss, Sensorineural* / genetics
Humans
Keratoderma, Palmoplantar* / complications
Keratoderma, Palmoplantar* / genetics
Mutation
Pedigree

Substances

Connexins

Supplementary concepts

Palmoplantar Keratoderma with Deafness