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Nagashima-type palmoplantar keratoderma: Case series and two novel variants
Mitchell Braun1, Keith A Choate2, Erin F Mathes3
1University of California San Francisco School of Medicine, San Francisco, California, USA.
Abstract:
Nagashima-type palmoplantar keratoderma (PPK) is an autosomal recessive PPK. We report four patients, highlight two new genetic variants, and emphasize the possibility of misdiagnosing the condition. Concomitant atopic dermatitis, specifically, may make correct diagnosis challenging. Clinicians should consider the diagnosis of Nagashima-type PPK in patients presenting with mild PPK with transgrediens and understand the importance of individualized multimodal treatment regimens.
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