Arrhythmogenic right ventricular dysplasia causes: Difference between revisions
Jump to navigation
Jump to search
Hudakarman (talk | contribs) |
Hudakarman (talk | contribs) (→Causes) |
||
| Line 4: | Line 4: | ||
==Causes== | ==Causes== | ||
Arrhythmogenic right ventricular cardiomyopathy is cause by genetic inheritance as: | |||
* An autosomal dominant pattern with variable penetrance and incomplete expression. | |||
* A mutation in genes encoding a desmosome protein ( 40% to 50% of ARVC/D patients) | |||
* The gene is on the chromosome 14q23-q24 | |||
* There is an autosomal recessive trait variant associated with palmoplantar keratosis and wooly hair named Naxos disease | |||
Revision as of 15:09, 20 May 2020
Overview
Arrhythmogenic right ventricular cardiomyopathy is typically inherited as an autosomal dominant pattern with variable penetrance and incomplete expression. Approximately 40% to 50% of ARVC/D patients have a mutation in genes encoding a desmosome protein. The gene is on the chromosome 14q23-q24.There is an autosomal recessive trait variant associated with palmoplantar keratosis and wooly hair named Naxos disease.
Causes
Arrhythmogenic right ventricular cardiomyopathy is cause by genetic inheritance as:
- An autosomal dominant pattern with variable penetrance and incomplete expression.
- A mutation in genes encoding a desmosome protein ( 40% to 50% of ARVC/D patients)
- The gene is on the chromosome 14q23-q24
- There is an autosomal recessive trait variant associated with palmoplantar keratosis and wooly hair named Naxos disease