Lown-Ganong-Levine Syndrome

Watchlist

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Retrieved

2021-01-23

Source

Orphanet

Trials

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Genes

TRBV20OR9-2, B3GAT1, FCGR3A, FCGR3B, GEM, KIR3DL1, STAT3, CNTN2, TNF

Drugs

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Lown-Ganong-Levine syndrome is an extremely rare conduction disorder characterized by a short PR interval (less than or equal to 120 ms) with normal QRS complex on electrocardiogram associated with the occurrence of episodes of atrial tachyarrythmias (e.g. atrial fibrillation, atrial tachycardia).