infantile histiocytoid Cardiomyopathy
A rare cardiomyopathy with onset usually before age 2; generally, more females are affected than males. It is characterized by the presence of pale granular foamy cells that resemble HISTIOCYTES within the MYOCARDIUM. Infants present with sudden onset dysrhythmia or cardiac arrest, similar to SIDS. It may be associated with mutations in the electron transport complex III, cytochrome b (MTCYB) gene. OMIM: 500000
Also Known As:
Cardiomyopathy, infantile histiocytoid; Cardiomyopathy, Focal Lipid; Cardiomyopathy, Infantile Xanthomatous; Cardiomyopathy, Oncocytic; Foamy myocardial transformation of infancy; Focal lipid cardiomyopathy; Infantile xanthomatous cardiomyopathy; Oncocytic cardiomyopathy
Networked: 3
relevant articles (0 outcomes,
0 trials/studies)
Disease Context: Research Results
Related Diseases
Experts
1. | Brown, M D:
1 article
(09/2004)
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2. | Jeven, G:
1 article
(09/2004)
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3. | Vallance, H D:
1 article
(09/2004)
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4. | Wallace, D C:
1 article
(09/2004)
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5. | Dvorák, K:
1 article
(01/2004)
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6. | Feit, J:
1 article
(01/2004)
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7. | Hermanová, M:
1 article
(01/2004)
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8. | Hotárková, S:
1 article
(01/2004)
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9. | Hucín, B:
1 article
(01/2004)
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10. | Jicínská, H:
1 article
(01/2004)
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Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to infantile histiocytoid Cardiomyopathy: