Histiocytoid cardiomyopathy (Q95446): Difference between revisions
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A cardiomiopatia histiocitoide é uma doença genética rara que afeta principalmente meninas na primeira infância devida a um distúrbio mitocondrial. É caracterizada por cardiomiopatia dilatada, arritmias cardíacas graves ou morte súbita. O miocárdio demonstra crescimento anormal de células de Purkinje e a presença de células semelhantes a histiócitos. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
