Porokeratotic eccrine nevus may be caused by somatic connexin26 mutations

Jennifer A. Easton, Steven Donnelly, Miriam A F Kamps, Peter M. Steijlen, Patricia E. Martin, Gianluca Tadini, René Janssens, Rudolf Happle, Michel Van Geel, Maurice A M Van Steensel

Research output: Contribution to journalArticle

Abstract

Porokeratotic eccrine ostial and dermal duct nevus, or porokeratotic eccrine nevus (PEN), is a hyperkeratotic epidermal nevus. Several cases of widespread involvement have been reported, including one in association with the keratitis-ichthyosis-deafness (KID) syndrome (OMIM #148210), a rare disorder caused by mutations in the GJB2 gene coding for the gap junction protein connexin26 (Cx26). The molecular cause is, as yet, unknown. We have noted that PEN histopathology is shared by KID. The clinical appearance of PEN can resemble that of KID syndrome. Furthermore, a recent report of cutaneous mosaicism for a GJB2 mutation associated with KID describes linear hyperkeratotic skin lesions that might be consistent with PEN. From this, we hypothesized that PEN might be caused by Cx26 mutations associated with KID or similar gap junction disorders. Thus, we analyzed the GJB2 gene in skin samples from two patients referred with generalized PEN. In both, we found GJB2 mutations in the PEN lesions but not in unaffected skin or peripheral blood. One mutation was already known to cause the KID syndrome, and the other had not been previously associated with skin symptoms. We provide extensive functional data to support its pathogenicity. We conclude that PEN may be caused by mosaic GJB2 mutations.

Original languageEnglish
Pages (from-to)2184-2191
Number of pages8
JournalJournal of Investigative Dermatology
Volume132
Issue number9
DOIs
Publication statusPublished - Sep 2012

Fingerprint

Nevus
Skin
Mutation
Genes
Connexins
Ducts
Blood
Genetic Databases
Mosaicism
Gap Junctions
Virulence
Keratitis-Ichthyosis-Deafness Syndrome

ASJC Scopus subject areas

  • Dermatology
  • Biochemistry
  • Cell Biology
  • Molecular Biology

Cite this

Easton, J. A., Donnelly, S., Kamps, M. A. F., Steijlen, P. M., Martin, P. E., Tadini, G., ... Van Steensel, M. A. M. (2012). Porokeratotic eccrine nevus may be caused by somatic connexin26 mutations. Journal of Investigative Dermatology, 132(9), 2184-2191. https://doi.org/10.1038/jid.2012.143

Porokeratotic eccrine nevus may be caused by somatic connexin26 mutations. / Easton, Jennifer A.; Donnelly, Steven; Kamps, Miriam A F; Steijlen, Peter M.; Martin, Patricia E.; Tadini, Gianluca; Janssens, René; Happle, Rudolf; Van Geel, Michel; Van Steensel, Maurice A M.

In: Journal of Investigative Dermatology, Vol. 132, No. 9, 09.2012, p. 2184-2191.

Research output: Contribution to journalArticle

Easton, JA, Donnelly, S, Kamps, MAF, Steijlen, PM, Martin, PE, Tadini, G, Janssens, R, Happle, R, Van Geel, M & Van Steensel, MAM 2012, 'Porokeratotic eccrine nevus may be caused by somatic connexin26 mutations', Journal of Investigative Dermatology, vol. 132, no. 9, pp. 2184-2191. https://doi.org/10.1038/jid.2012.143
Easton, Jennifer A. ; Donnelly, Steven ; Kamps, Miriam A F ; Steijlen, Peter M. ; Martin, Patricia E. ; Tadini, Gianluca ; Janssens, René ; Happle, Rudolf ; Van Geel, Michel ; Van Steensel, Maurice A M. / Porokeratotic eccrine nevus may be caused by somatic connexin26 mutations. In: Journal of Investigative Dermatology. 2012 ; Vol. 132, No. 9. pp. 2184-2191.
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