γ-secretase mutations in hidradenitis suppurativa: New insights into disease pathogenesis

136Citations
Citations of this article
153Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Hidradenitis suppurativa (HS) is a debilitating chronic inflammatory skin condition of unclear etiology. It may segregate as an autosomal dominant trait, and heterozygous mutations in the γ-secretase genes NCSTN, PSENEN, and PSEN1 have recently been reported in a small number of multiplex kindreds and sporadic cases. These mutations highlight γ-secretase (an enzyme that has been extensively investigated in familial Alzheimer's disease) to have an integral role in cutaneous biology and, more specifically, in HS. In this article, we review the recent genetic data, how they inform disease pathogenesis, and the long-term implications in HS and related diseases. © 2013 The Society for Investigative Dermatology.

Cite

CITATION STYLE

APA

Pink, A. E., Simpson, M. A., Desai, N., Trembath, R. C., & Barker, J. N. W. (2013). γ-secretase mutations in hidradenitis suppurativa: New insights into disease pathogenesis. Journal of Investigative Dermatology, 133(3), 601–607. https://doi.org/10.1038/jid.2012.372

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free