Medical

arrhythmogenic right ventricular dysplasia type 9

An autosomal dominant condition (OMIM:609040) characterised by fibro-fatty degeneration of the right ventricular myocardium, electromechanical instability and sudden death.

Molecular pathology
Defects in PKP2 cause arrhythmogenic right ventricular dysplasia type 9.

Mentioned in

accordion sign
arrhythmogenic right ventricular dysplasia
arrhythmogenic right ventricular dysplasia type 10
arrhythmogenic right ventricular dysplasia type 5
DSG2
Naxos Disease
PKP2
right ventricular dysplasia
ryanodine receptor 2
RYR2
TGFB3
woolly hair disease
Woolly Hair Syndrome

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