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Netherton Syndrome: Insights into Pathogenesis and Clinical Implications
Elena Chiticariu1, Daniel Hohl1
1Service of Dermatology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Abstract:
Netherton syndrome (NS) is a rare skin disorder involving the skin, hair, and immune system. Pathological manifestations are due to unopposed kallikrein peptidase activity because of a SPINK5 gene deficiency. In their article, Gouin et al. explore the role of kallikrein 14 in the stratum granulosum, defining it as an important player implicated in the pathogenesis of NS hair shaft anomalies.
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