Late presentation of Ellis van Creveld Syndrome with Common atrium anomaly: A case report in a Nepalese Adult

A. Hirachan, K. Bishal, A. Maskey, Madhu Roka, G. Hirachan
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Abstract

Ellis Van Creveld syndrome (EVC) is a rare genetic disorder having autosomal recessive inheritance characterized by chondrodystrophy, polydactyly, ectodermal dysplasia, and various cardiac anomalies. Acromelic shortening of upper and lower limbs, genu valgum, deformed teeth, short ribs and narrow thorax and other systemic anomalies complete the picture of this syndrome. The patients with the syndrome rarely survive into adulthood. Here, we report a 30 year old male with EVC presenting for the first time in middle age with Common atrium anomaly.
晚期Ellis van Creveld综合征伴常见心房异常:尼泊尔成人一例报告
Ellis Van Creveld综合征(EVC)是一种罕见的常染色体隐性遗传遗传病,以软骨营养不良、多指畸形、外胚层发育不良和各种心脏异常为特征。上肢和下肢肢端曲性缩短、膝外翻、牙齿变形、肋骨短、胸窄以及其他系统性异常都是本综合征的表现。患有这种综合症的病人很少能活到成年。在此,我们报告一位30岁男性EVC在中年首次出现,并伴有常见的心房异常。
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