Myocardial Disease: Difference between revisions

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† A pathogenic mutation is a DNA alteration associated with ARVC/D that alters or is expected to alter the encoded protein, is unobserved or rare in a large non–ARVC/D control population, and either alters or is predicted to alter the structure or function of the protein or has demonstrated linkage to the disease phenotype in a conclusive pedigree. E.g.: in TMEM43, DSP, PKP2, DSG2, DSC2, JUP.  
† A pathogenic mutation is a DNA alteration associated with ARVC/D that alters or is expected to alter the encoded protein, is unobserved or rare in a large non–ARVC/D control population, and either alters or is predicted to alter the structure or function of the protein or has demonstrated linkage to the disease phenotype in a conclusive pedigree. E.g.: in TMEM43, DSP, PKP2, DSG2, DSC2, JUP.  
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<gallery>
Image:arvd_ecg1.png| a patient with ARVD
Image:arvd_ecg2.png
Image:arvd_ecg3.png
</gallery>
====Treatment====
====Treatment====
Treatment focuses on avoiding complications.  
Treatment focuses on avoiding complications.  

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