Key result
Idiopathic dilated cardiomyopathy is a condition of obscure etiology that may be associated with multiple immunologic defects, autoimmunity, and undiagnosable viral infections.
The paper discusses the potential immunologic, genetic, and infectious etiologies underlying idiopathic dilated cardiomyopathy.
Answers are grounded in this paper and cite their sources.
Does not alter management of idiopathic dilated cardiomyopathy; leaves open causal mechanisms and targeted therapies for future study.
Third New International Dictio- nary defines "idiopathic" as "arising spontaneously or from an obscure or un- known cause." Medical diagnostic terminology has included this adjective for many years,' and its mys- terious nature has survived into the current era of sophisticated technology and molecular analyses. Id- iopathic dilated cardiomyopathy (IDC) is character- ized by increased left ventricular intracavitary dimen- sions, reduced systolic function, and, commonly, a congestive heart failure syndrome, but IDC is with- out a clear-cut etiology. Within the context of idiopathy, attempts have been made to associate IDC with various medical entities frequently connected to ill- nesses of obscure origin; for example, with autoim- munity and undiagnosable viral infections. In fact, numerous results indicating multiple immunologic defects have been generated from patients with IDC.
No takes yet. Share an insight, caveat, or question.
Jeremy Bender (1991) conducted a review in Idiopathic dilated cardiomyopathy. Idiopathic dilated cardiomyopathy is a condition of obscure etiology that may be associated with multiple immunologic defects, autoimmunity, and undiagnosable viral infections.
Synapse has enriched 10 related papers. Consider them for comparative context: