Histiocytoid cardiomyopathy (Q95446): Difference between revisions

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Latest revision as of 11:13, 16 August 2026

Histiocytoid cardiomyopathy is a rare genetic condition primarily affecting girls in early childhood due to a mitochondrial disorder. It is characterised by dilated cardiomyopathy, severe cardiac arrhythmias or sudden death. The myocardium demonstrates abnormal growth of Purkinje cells and the presence of a histiocyte-like cells.

Language	Label	Description	Also known as
default for all languages	ID_1870618141
English	Histiocytoid cardiomyopathy	Histiocytoid cardiomyopathy is a rare genetic condition primarily affecting girls in early childhood due to a mitochondrial disorder. It is characterised by dilated cardiomyopathy, severe cardiac arrhythmias or sudden death. The myocardium demonstrates abnormal growth of Purkinje cells and the presence of a histiocyte-like cells.