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Congenital Idiopathic Dilatation of the Right Atrium: Antenatal Appearance, Postnatal Management, Long-Term Follow-Up and Possible Pathomechanism
Author(s) -
Sigrun R. Hofmann,
Antje Heilmann,
Hans J. Häusler,
Ingo Dähnert,
G Kamin,
Robert Lachmann
Publication year - 2012
Publication title -
fetal diagnosis and therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.976
H-Index - 60
eISSN - 1421-9964
pISSN - 1015-3837
DOI - 10.1159/000338661
Subject(s) - medicine , cardiology , thrombus , abnormality , atrium (architecture) , atrial fibrillation , psychiatry
Idiopathic dilatation of the right atrium (IDRA) is a rare abnormality usually detected by chance at any time between antenatal and adult life. It is defined as isolated enlargement of the right atrium in the absence of other cardiac lesions causing right atrial dilatation. IDRA can be associated with atrial arrhythmia and systemic embolism. The clinical presentation shows high variability ranging from the lack of any symptoms up to cardiac failure.

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