Quadricuspid Aortic Valve, Single Coronary Artery, Solitary Kidney and Oblique Facial Cleft. A Unique Constellation of Congenital Abnormalities: Case Report and Review of the Literature

Rabah Al-Mehisen, Ramy El Essely, M. Al-Mallah, M. Al-Mohaissen, T. Kashour
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引用次数: 4

Abstract

Quadricuspid aortic valve (QAV) is a rare congenital anomaly which is associated with coronary artery anomalies in 10% of the patients. The association of QAV with single coronary artery (SCA) is very rare has been reported only in one case previously. We report the case of a 30-year-old male patient with a unique constellation of congenital anomalies including QAV, SCA, solitary kidney and Tessier type 3 oblique facial cleft with cleft palate. To our knowledge, this unique combination has never been described previously. We describe his case and review the topic of QAV and its reported cardiac and systemic associations.
四尖瓣主动脉瓣,单冠状动脉,孤立肾和斜面裂。先天性畸形的独特星座:病例报告和文献回顾
四尖瓣主动脉瓣(QAV)是一种罕见的先天性异常,在10%的患者中与冠状动脉异常有关。QAV与单冠状动脉(SCA)的关联非常罕见,此前仅报道一例。我们报告一例30岁的男性患者,先天性异常包括QAV, SCA,孤立肾和Tessier型3斜面裂合并腭裂。据我们所知,这种独特的组合以前从未被描述过。我们描述了他的病例,并回顾了QAV的主题及其报道的心脏和全身关联。
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