Histiocytoid cardiomyopathy (Q95446): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
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. |
Statements
CID11:ID_1870618141
0 references
dki-india-ID_1870618141
0 references
Concluído
0 references
15 August 2026
0 references
