Lutembacher's syndrome: Difference between revisions
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==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
This is a very rare disease. The incidence is 0.001/1000000<ref name="pmid3354470">{{cite journal| author=Berry NS, Bauman JL, Gallastegui JL, Bauma W, Beckman KJ, Hariman RJ| title=Analysis of antiarrhythmic drug concentrations determined during electrophysiologic drug testing in patients with inducible tachycardias. | journal=Am J Cardiol | year= 1988 | volume= 61 | issue= 11 | pages= 922-4 | pmid=3354470 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3354470 }} </ref>. | |||
==Risk Factors== | ==Risk Factors== | ||
Revision as of 21:07, 6 August 2013
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Lutembacher's syndromeis a rare form of congenital heart disease. It refers to a combination of congenital atrial septal defect complicated by an acquired mitral stenosis.
Classification
Pathophysiology
Epidemiology and Demographics
This is a very rare disease. The incidence is 0.001/1000000[1].
Risk Factors
Natural history, Complications and Prognosis
References
- ↑ Berry NS, Bauman JL, Gallastegui JL, Bauma W, Beckman KJ, Hariman RJ (1988). "Analysis of antiarrhythmic drug concentrations determined during electrophysiologic drug testing in patients with inducible tachycardias". Am J Cardiol. 61 (11): 922–4. PMID 3354470.