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首页> 外文期刊>Heart and vessels: An international journal >Mitral regurgitation without supravalvular aortic stenosis in Williams syndrome.
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Mitral regurgitation without supravalvular aortic stenosis in Williams syndrome.

机译:Williams综合征中无二尖瓣关闭不全的二尖瓣关闭不全。

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Isolated mitral regurgitation without supravalvular aortic stenosis is rarely identified in Williams syndrome. We describe the case of a 24-year-old man with isolated mitral regurgitation in Williams syndrome. Severe regurgitation due to prolapse of the anterior leaflet was noted in an echocardiogram and color Doppler, and a left ventriculogram showed grade IV regurgitation. No pressure gradient between the left ventricle and the ascending aorta was found. Mitral regurgitation had been noted since his birth, and pediatricians suspected Williams syndrome because of postnatal growth deficiency, mental deficiency, unusual personality, and unusual facial features in his childhood. The diagnosis was confirmed by demonstration of the hemizygous deletion of 7q11.23 in the karyotype by the fluorescent in situ hybridization technique after his admission to our department. The patient underwent mitral valve replacement, and microscopic examination of the excised valve revealed myxomatous degeneration.
机译:在威廉姆斯综合征中很少发现没有瓣上主动脉瓣狭窄的孤立性二尖瓣关闭不全。我们描述了一个患有威廉姆斯综合征的二尖瓣关闭不全的24岁男子的病例。在超声心动图和彩色多普勒检查中发现由于前小叶脱垂而引起的严重反流,左心室示为IV级反流。在左心室和升主动脉之间未发现压力梯度。自他出生以来就已注意到二尖瓣关闭不全,儿科医生怀疑威廉姆斯综合症是由于出生后生长发育不足,智力不足,性格异常和童年时期的异常面部特征。入院后,通过荧光原位杂交技术证实了核型7q11.23的半合子缺失,证实了诊断。患者接受二尖瓣置换术,切除的瓣膜镜检发现粘液样变性。

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