familial atrial fibrillation


familial atrial fibrillation

A rare autosomal-dominant condition characterised by a family pedigree of atrial fibrillation associated with defined ion channel abnormalities, especially sodium channels.

familial atrial fibrillation

A rare autosomal dominant disease caused by a mutation on chromosome 10. The features of the disease do not appear to differ from those of common ATRIAL FIBRILLATION.