Histiocytoid cardiomyopathy (Q95446): Difference between revisions
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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. |
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CID11:ID_1870618141
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dki-india-ID_1870618141
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