PMID: 8113158Jan 1, 1994

Absent aortic and pulmonary valves: investigation of three fetal cases with cystic hygroma and review of the literature

Heart and Vessels
S MiyabaraH Sugihara

Abstract

Absent semilunar valve was found in three fetal cases with cystic hygroma. Two cases which simultaneously showed absent aortic and pulmonary valves (AAV and APV, respectively) had double-outlet right ventricle. The third case, which lacked only the aortic valve, had atrioventricular septal defect and anomalous origin of the right subclavian artery. Two of the three cases had a markedly hypoplastic thymus. Fifteen AAV and 179 APV cases, including the above-mentioned cases and others reported elsewhere, were discussed with special reference to the pathogenesis of absent semilunar valve. Of the 15 AAV cases, hypoplasia of the left heart was observed in 11 cases (73.3%), double-outlet right ventricle in 5 (33.3%), and aortic arch malformations in 6 (40.0%). In the 179 APV cases, there were 111 tetralogy of Fallot (62.0%) and 44 right-sided aortic arch (24.6%). DiGeorge anomaly was found in one AAV and eight APV cases. These results indicate a pathogenesis that is possibly related to hemodynamic abnormalities or abnormal neural crest cells. Further investigation will be needed to elucidate a more definite pathogenesis of absent semilunar valve.

References

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Jan 15, 2019·Journal of Medical Ultrasonics·Shui-Hua YangHong-Wei Wei
Jan 20, 1997·American Journal of Medical Genetics·S MiyabaraH Sugihara
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Related Concepts

AAVS1
Embryopathies
Pathogenesis
Antenatal Screening Procedures
Hypoplasia
Pulmonary Valve Structure
Atrioventricular CANAL Defect
Aortic Arch Structure
Evaluation
Right

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