Lebecque P, Bosi G, Lintermans J, Stijns M, Germanes J, Chalant C H, Vliers A
Eur J Pediatr. 1984 Feb;141(4):228-30. doi: 10.1007/BF00572766.
This a report of myxomatous mitral valve degeneration in a child with Turner syndrome. The diagnosis was first suspected at 7 months of age. At 5 years of age, ultrasonic and angio-cardiographic confirmation prompted a successful mitral valve replacement with a Starr prosthesis. The child also had partial anomalous pulmonary venous return and a dysplastic right kidney. The child has remained well for 4 years after surgery.
这是一篇关于一名患有特纳综合征儿童的黏液瘤样二尖瓣退变的报告。该诊断最初在患儿7个月大时被怀疑。5岁时,超声心动图和心血管造影检查确诊后,成功地用斯塔尔人工瓣膜进行了二尖瓣置换术。该患儿还存在部分肺静脉异位回流和右肾发育不良。术后该患儿已健康存活4年。