Comprehensive pathological and genetic investigation of three young adult myotonic dystrophy type 1 patients with sudden unexpected death

Hata, Yukiko; Ichimata, Shojiro; Yoshida, Kōji; Yamaguchi, Yoshiaki; Hirono, Keiichi; Nishida, Naoki

doi:10.1007/s00415-023-11850-8

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Sudden Cardiac Death1

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2024

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“…Independent predictors of SCD are (i) clinical diagnosis of atrial tachyarrhythmia and electrocardiogram (ECG) with one of the following features: any rhythm other than sinus rhythm, PR interval ≥ 240 ms, QRS duration ≥ 120 ms, second-or third-degree atrioventricular block [37,39], age, family history of SCD, and left bundle branch block [40,41].…”

Section: Sudden Cardiac Deathmentioning

confidence: 99%

Comprehensive Cardiovascular Management of Myotonic Dystrophy Type 1 Patients: A Report from the Italian Neuro-Cardiology Network

Russo,

Antonini,

Massa

et al. 2024

JCDD

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Myotonic dystrophy is a hereditary disorder with systemic involvement. The Italian Neuro-Cardiology Network (INCN-RNC) is a unique collaborative experience involving neurology units combined with cardio-arrhythmology units. The INCN facilitates the creation of integrated neuro-cardiac teams in Neuromuscular Disease Centers for the management of cardiovascular involvement in the treatment of myotonic dystrophy type 1 (MD1).

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