From Mdwiki | Naxos disease | |
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| Other names: Diffuse non-epidermolytic palmoplantar keratoderma with woolly hair and cardiomyopathy | |
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| Cutaneous phenotype of Naxos disease: woolly hair (A), palmar (B) and plantar (C) keratoses. | |
Naxos disease (also known as "diffuse non-epidermolytic palmoplantar keratoderma with woolly hair and cardiomyopathy,"[1] "diffuse palmoplantar keratoderma with woolly hair and arrhythmogenic right ventricular cardiomyopathy, first described on the island of Naxos by Nikos Protonotarios,"[1] and "Naxos disease"[1]) is a cutaneous condition characterized by a palmoplantar keratoderma.[1] The prevalence of the syndrome is up to 1 in every 1000 people in the Greek islands.[2]
It has been associated with mutations in the genes encoding the proteins desmoplakin, plakoglobin, desmocollin-2, and SRC-interacting protein (SIP).[3][4] A variation of Naxos syndrome is known as Carvajal syndrome.[2]
Between 80 and 99% of those with Naxos disease will display some of the following symptoms:r[5]
The desmosomal proteins plakoglobin and desmoplakin take on mutations that cause Naxos disease. [6]
Increased mechanical stress leads to cell death, due to defects in linking sites of plakoglobin and desmoplakin which can interrupt series of cell adhesion[6]
The treatment for this condition is based on the following:[6]
| Classification |
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Categories: [Genodermatoses] [Palmoplantar keratodermas] [Syndromes]