Naxos disease

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Cutaneous phenotype of Naxos disease: woolly hair (A), palmar (B) and plantar (C) keratoses.

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Naxos disease is an autosomal recessive variant of ARVD, described initially on the Greek island of Naxos. There, the penetrance is >90%.

It involves the gene that codes for plakoglobin (a protein that is involved in cellular adhesion), on chromosome 17p.

Naxos disease is described as a triad of ARVD, palmoplantar keratosis, and wooly hair.

The signs of Naxos disease are more severe than with autosomal dominant ARVD.

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