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Article

Characterising heart rhythm abnormalities associated with Xp22.31 deletion

15 Nov 2022

Abstract excerpt

Background Genetic deletions at Xp22.31 are associated with the skin condition X linked ichthyosis (XLI), and with a substantially increased risk of atrial fibrillation/flutter (AF), in males. AF is associated with elevated thrombosis, heart failure, stroke and dementia risk. Methods Through: (a) examining deletion carriers with a diagnosis of AF in UK Biobank, (b) undertaking an online survey regarding abnormal...

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PMID: 36379544
DOI: 10.1136/jmg-2022-108862

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