Autosoomne dominantne
Perekondades esinev kodade virvendus, mis on seotud muutustega geenides nagu KCNQ1, KCNJ2, GJA5, MYL4, NPPA ja SCN5A.
Mida diagnoos muudab
Sellest teadmine toetab sugulaste varasemat EKG-kontrolli ning insuldi ennetamise õigeaegset arutamist.
Tuntud ka nimetustena
atrial fibrillation autosomal dominant; atrial fibrillation, familial; hereditary atrial fibrillation (disease)
Hõlmab 20 seotud alatüüpi ↓Peida alatüübid ↑
- atrial fibrillation, familial, 1
- atrial fibrillation, familial, 10
- atrial fibrillation, familial, 11
- atrial fibrillation, familial, 12
- atrial fibrillation, familial, 13
- atrial fibrillation, familial, 14
- atrial fibrillation, familial, 15
- atrial fibrillation, familial, 16
- atrial fibrillation, familial, 17
- atrial fibrillation, familial, 18
- atrial fibrillation, familial, 2
- atrial fibrillation, familial, 3
- atrial fibrillation, familial, 4
- atrial fibrillation, familial, 5
- atrial fibrillation, familial, 6
- atrial fibrillation, familial, 7
- atrial fibrillation, familial, 8
- atrial fibrillation, familial, 9
- Brugada syndrome 7
- long QT syndrome 10
