Histiocytoid cardiomyopathy

Histiocytoid cardiomyopathy is an arrhythmogenic disorder characterised by cardiomegaly, severe cardiac arrhythmias or sudden death, and the presence of histiocyte-like cells within the myocardium.

Wolff-Parkinson-White syndrome

A disorder of the cardiac conduction system of the heart characterized by ventricular preexcitation due to the presence of an abnormal accessory atrioventricular electrical conduction pathway.


Total: 2

                       


(per page)
PMID (PMCID)
24438356
 FEMALE Infant, Newborn
The perfect storm? Histiocytoid cardiomyopathy and compound CACNA2D1 and RANGRF mutation in a baby.
Cataldo S, Annoni GA, Marziliano N.
Cardiol Young. 2015;25(1):174-6.
A female baby suffered from a rare association between histiocytoid cardiomyopathy, left ventricular non-compaction, and Wolff-Parkinson-White syndrome causing severe and recurrent arrhythmic storms.
3310564
 FEMALE Infant
Oncocytic cardiomyopathy of infancy with Wolff-Parkinson-White syndrome and ectopic foci causing tachydysrhythmias in children.
Keller BB, Mehta AV, Shamszadeh M, Marino TA, Sanchez GR, Huff DS, Dunn JM.
Am Heart J. 1987;114(4 Pt 1):782-92.
Oncocytic cardiomyopathy of infancy with Wolff-Parkinson-White syndrome and ectopic foci causing tachydysrhythmias in children.