Congenital tricuspid stenosis

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A rare congenital tricuspid malformation characterized by narrowing of the tricuspid valve orifice due to congenital valve anomalies such as incompletely developed leaflets shortened and malformed chordae tendineae small annulus and/or abnormal number and size of papillary muscles resulting in right ventricular inflow obstruction. Clinical presentation depends on the degree of stenosis as well as the presence or absence of additional cardiac anomalies and includes easy fatigability swelling of the lower limbs and hepatomegaly among others.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on Data version July 2024

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Congenital tricuspid stenosis?

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