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The Proteolytic Network in Palmoplantar Keratoderma: SERPINA12 Joins the Family
Lloyd Steele1, Soha S Tawfik2, Edel A O'Toole1
1Department of Dermatology, The Royal London Hospital, Barts Health NHS Trust, ERN-Skin, London, United Kingdom; Centre for Cell Biology and Cutaneous Research, Blizard Institute, Queen Mary University of London, London, United Kingdom.
Abstract:
Mohamad et al. (2020) describe loss-of-function mutations in SERPINA12 as a cause of diffuse, transgradient palmoplantar keratoderma (PPK). This disorder shares similar clinical features with other PPKs caused by protease overactivity, including erythema, peeling, and exacerbation on water exposure. Understanding this disorder may shed further light on the role of proteases and their inhibitors in epidermal physiology.
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