scholarly journals Parachute mitral valve and Pacman deformity of the ventricular septum in a middle-aged male

2016 ◽  
Vol 68 ◽  
pp. S126-S130 ◽  
Author(s):  
Jagdish C. Mohan ◽  
Madhu Shukla ◽  
Vishwas Mohan ◽  
Arvind Sethi
2018 ◽  
Author(s):  
Branka Sosic-Jurjevic ◽  
Dieter Lutjohann ◽  
Dragana Miljic ◽  
Jasmina Ciric ◽  
Svetlana Trifunovic ◽  
...  

2020 ◽  
Vol 1 (6) ◽  
pp. 1736-1737
Author(s):  
David J. Carlberg ◽  
Michael C. Izzo ◽  
Jonathan E. Davis

2012 ◽  
Vol 41 (3) ◽  
pp. 601-609 ◽  
Author(s):  
Ilia Kritikou ◽  
Maria Basta ◽  
Rafel Tappouni ◽  
Slobodanha Pejovic ◽  
Julio Fernandez-Mendoza ◽  
...  

1969 ◽  
Vol 77 (6) ◽  
pp. 809-813 ◽  
Author(s):  
Allan L. Simon ◽  
William F. Friedman ◽  
William C. Roberts

Circulation ◽  
2020 ◽  
Vol 142 (Suppl_3) ◽  
Author(s):  
uzoma obiaka ◽  
Anna Chow ◽  
Jen Lie Yau ◽  
Valeria Matto Morina ◽  
Shubhika Srivastava

Background: The incidence of congenital mitral valve disease is 0.4%; Double Orifice Mitral Valve (DOMV) and Parachute Mitral Valve (PMV) are two morphologic pathologies that may result in mitral valve dysfunction. The objectives of this study are 1) To describe valve function and progression and 2) To define factors contributing to disease progression. Methods: Retrospective database review. Fyler codes for DOMV, PMV and text search was performed. Echocardiographic images, echo reports, and chart review were used to identify mitral regurgitation (MR), mitral stenosis (MS), morphology, and associated lesions. Results: 39 patients with DOMV and 76 patients with PMV were identified. In the DOMV cohort, 51% were male, median age at diagnosis was 0.17 years (IQR 0.01, 3.88); median follow-up of 5.92 years (IQR 0.46, 10.22). In the PMV cohort, 44% were male, median age at diagnosis at was 0.01 years (IQR 0, 0.34); median follow-up of 2.56 years (IQR 0.25, 9.55). 41% of DOMV and 23% of patients with PMV had normal valve function at initial visit. DOMV was associated with MR (p=0.04), and PMV with MS (p<0.0001). 23% of patients in the PMV cohort had progressive MS compared to 5% of patients in the DOMV cohort (p<0.0001). There was no significant difference in MR progression between both groups (p=0.02). Papillary muscle (PM) morphology was evaluated in 37 (excluding canals) of 76 patients in the PMV cohort. 5 had true PMV (single PM), 32 had variant PMV with two PM groups of which 62.5% had dominant posterior medial PM. 67% of those with posterior medial PM dominance had progressive MS irrespective of association with Shone’s complex. The anterolateral PM muscle group dominant PMV were not associated with Shone’s complex and progressive MS. Conclusion: DOMV are more likely to have MR while PMV are more likely to have MS. DOMV has non progressive MR and MS. Posterior medial PM dominance in PMV is more likely to have progressive MS.


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