Left Atrial Isomerism in Afro-Caribbean Adolescents and Adults with no Intervention: Echocardiographic Findings.

S. Williams-Phillips, M. Hoo Sang
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Abstract

Left atrial isomerism (LAI) is a rare congenital anomaly usually associated with major or minor congenital cardiac lesions. Presentation beyond childhood is unusual as there is usually high morbidity of 63% associated with the co-morbid major congenital cardiac lesions in the first year of life. The four index cases highlight the myriad cardiac lesions facilitating survival into adolescence and adulthood of this rare cardiac condition. Presented are markedly different echocardiographic findings of four cases of LAI in Afro-Caribbeans who had no intervention. Their diagnostic transthoracic echocardiographic findings are the focussed features of this article and the first documentation of isolated patent ductus arteriosus with LAI. Fascinating diagnostic chest X-ray findings of the LAI index cases are presented. They are the first cases of LAI documented in Afro-Caribbeans.
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非裔加勒比青少年和成人的左心房异构体不经干预:超声心动图结果。
左房异构体(LAI)是一种罕见的先天性异常,通常与或大或小的先天性心脏病变有关。儿童期以后的表现是不寻常的,因为通常有63%的高发病率与生命第一年合并的主要先天性心脏病变有关。这四个指数病例突出了无数的心脏病变,促进了这种罕见心脏疾病进入青春期和成年期的生存。本文介绍了4例未经干预的非洲-加勒比地区LAI患者的超声心动图表现。他们的经胸超声心动图诊断结果是本文的重点特点,也是孤立性动脉导管未闭伴LAI的首次文献记录。介绍了LAI指数病例的迷人诊断胸部x线表现。他们是非洲-加勒比地区记录的第一例LAI病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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