Naxos disease: Cardiocutaneous syndrome due to cell adhesion defect

<p>Abstract</p> <p>Naxos disease is a recessively inherited condition with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) and a cutaneous phenotype, characterised by peculiar woolly hair and palmoplantar keratoderma. The disease was first described in families o...

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Main Authors: Protonotarios Nikos, Tsatsopoulou Adalena
Format: Article
Language:English
Published: BMC 2006-03-01
Series:Orphanet Journal of Rare Diseases
Online Access:http://www.OJRD.com/content/1/1/4
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spelling doaj-8ceedf55b655440494d81466900d49de2020-11-24T20:59:03ZengBMCOrphanet Journal of Rare Diseases1750-11722006-03-0111410.1186/1750-1172-1-4Naxos disease: Cardiocutaneous syndrome due to cell adhesion defectProtonotarios NikosTsatsopoulou Adalena<p>Abstract</p> <p>Naxos disease is a recessively inherited condition with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) and a cutaneous phenotype, characterised by peculiar woolly hair and palmoplantar keratoderma. The disease was first described in families originating from the Greek island of Naxos. Moreover, affected families have been identified in other Aegean islands, Turkey, Israel and Saudi Arabia. A syndrome with the same cutaneous phenotype and predominantly left ventricular involvement has been described in families from India and Ecuador (Carvajal syndrome). Woolly hair appears from birth, palmoplantar keratoderma develop during the first year of life and cardiomyopathy is clinically manifested by adolescence with 100% penetrance. Patients present with syncope, sustained ventricular tachycardia or sudden death. Symptoms of right heart failure appear during the end stages of the disease. In the Carvajal variant the cardiomyopathy is clinically manifested during childhood leading more frequently to heart failure. Mutations in the genes encoding the desmosomal proteins plakoglobin and desmoplakin have been identified as the cause of Naxos disease. Defects in the linking sites of these proteins can interrupt the contiguous chain of cell adhesion, particularly under conditions of increased mechanical stress or stretch, leading to cell death, progressive loss of myocardium and fibro-fatty replacement. Implantation of an automatic cardioverter defibrillator is indicated for prevention of sudden cardiac death. Antiarrhythmic drugs are used for preventing recurrences of episodes of sustained ventricular tachycardia and classical pharmacological treatment for congestive heart failure, while heart transplantation is considered at the end stages.</p> http://www.OJRD.com/content/1/1/4
collection DOAJ
language English
format Article
sources DOAJ
author Protonotarios Nikos
Tsatsopoulou Adalena
spellingShingle Protonotarios Nikos
Tsatsopoulou Adalena
Naxos disease: Cardiocutaneous syndrome due to cell adhesion defect
Orphanet Journal of Rare Diseases
author_facet Protonotarios Nikos
Tsatsopoulou Adalena
author_sort Protonotarios Nikos
title Naxos disease: Cardiocutaneous syndrome due to cell adhesion defect
title_short Naxos disease: Cardiocutaneous syndrome due to cell adhesion defect
title_full Naxos disease: Cardiocutaneous syndrome due to cell adhesion defect
title_fullStr Naxos disease: Cardiocutaneous syndrome due to cell adhesion defect
title_full_unstemmed Naxos disease: Cardiocutaneous syndrome due to cell adhesion defect
title_sort naxos disease: cardiocutaneous syndrome due to cell adhesion defect
publisher BMC
series Orphanet Journal of Rare Diseases
issn 1750-1172
publishDate 2006-03-01
description <p>Abstract</p> <p>Naxos disease is a recessively inherited condition with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) and a cutaneous phenotype, characterised by peculiar woolly hair and palmoplantar keratoderma. The disease was first described in families originating from the Greek island of Naxos. Moreover, affected families have been identified in other Aegean islands, Turkey, Israel and Saudi Arabia. A syndrome with the same cutaneous phenotype and predominantly left ventricular involvement has been described in families from India and Ecuador (Carvajal syndrome). Woolly hair appears from birth, palmoplantar keratoderma develop during the first year of life and cardiomyopathy is clinically manifested by adolescence with 100% penetrance. Patients present with syncope, sustained ventricular tachycardia or sudden death. Symptoms of right heart failure appear during the end stages of the disease. In the Carvajal variant the cardiomyopathy is clinically manifested during childhood leading more frequently to heart failure. Mutations in the genes encoding the desmosomal proteins plakoglobin and desmoplakin have been identified as the cause of Naxos disease. Defects in the linking sites of these proteins can interrupt the contiguous chain of cell adhesion, particularly under conditions of increased mechanical stress or stretch, leading to cell death, progressive loss of myocardium and fibro-fatty replacement. Implantation of an automatic cardioverter defibrillator is indicated for prevention of sudden cardiac death. Antiarrhythmic drugs are used for preventing recurrences of episodes of sustained ventricular tachycardia and classical pharmacological treatment for congestive heart failure, while heart transplantation is considered at the end stages.</p>
url http://www.OJRD.com/content/1/1/4
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