A case of arrhythmogenic right ventricular cardiomyopathy—Naxos disease

Saravanan, R.; Amuthan, V; Janarthanan, R.A.; Balasubramanian, Sowmya; Smaoui, M.

doi:10.1016/s0019-4832(12)60017-0

Cited by 1 publication

(1 citation statement)

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“…Later, the disease was reported from other parts of the world including other Greek islands of Milos, Evia and Mykonos, Turkey, Israel, Saudi Arabia, India and Bangladesh [4,[9][10][11][12][13].…”

Section: Epidemiologymentioning

confidence: 99%

Cardiocutaneous Syndrome: The Tale between Heart and Skin

Islam¹,

Khan²,

Hossain³

2017

Glob J Rare Dis

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Cardiocutaneous syndromes are rare, genetically determined disorders in which arrhythmogenic cardiomyopathy is accompanied by characteristic cutaneous phenotypes of woolly hair and palmoplantar keratoderma. Pattern of cardiac involvement differs in different cardiocutaneous syndromes; right ventricle (RV) is predominantly affected in the form of classical arrhythmogenic right ventricular cardiomyopathy/ dysplasia (ARVC/D) in Naxos disease whereas the left ventricle (LV) is mainly involved in the form of dilated cardiomyopathy in Carvajal syndrome. Both conditions are transmitted in autosomal recessive manner, and results from mutations in cell adhesion molecules compromising the integrity of desmosomal junctions of skin and myocardium. Naxos disease usually presents by adolescence with malignant ventricular arrhythmia or cardiac arrest whereas Carvajal syndrome is manifested earlier with heart failure. Cardiomyopathy is diagnosed by the 2010 Task Force Criteria. Implantation of automated implantable cardioverter-defi brillator (AICD) forms the mainstays of treatment by preventing sudden cardiac death. Genetic testing is available. Several international databases and registries, often as a part of other genetically determined arrhythmogenic disorders, are directed to better characterize and manage these cardiocutaneous syndrome patients.

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Section: Epidemiologymentioning

confidence: 99%