特纳氏综合症中的心脏病

Helvetica paediatrica acta Pub Date : 1988-08-01
L Mazzanti, D Prandstraller, D Tassinari, I Rubino, S Santucci, F M Picchio, A Forabosco, E Cacciari
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引用次数: 0

摘要

对55例不同核型的特纳综合征患者进行了全面的心脏学评估(体格检查、心电图、胸部x线和超声心动图)。17%为先天性心脏病。与普通人群相比,只有主动脉缩窄和部分肺静脉引流异常的发生率显著高于普通人群(p < 0.001)。在特纳综合征患者的心脏异常中,以主动脉畸形(主动脉缩窄、主动脉狭窄、双尖主动脉)最为常见,其次为部分肺静脉异常引流,其发生率远高于文献报道。我们观察到,最严重的畸形最好发生在45,X,而环形模式的特点是发生率非常高的双尖主动脉。X同工染色体未见异常。
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Heart disease in Turner's syndrome.

Fifty-five consecutive patients with Turner's syndrome and different karyotypes underwent full cardiological evaluation (physical examination, electrocardiogram, chest X-ray and echocardiogram). Congenital heart disease was found in 17%. When compared with the general population, a significantly higher incidence was present only for aortic coarctation and partial anomalous pulmonary venous drainage (p less than 0.001). Among cardiac anomalies in Turner's syndrome patients, aortic malformations (aortic coarctation, aortic stenosis, bicuspid aorta) are the most frequent, followed by partial anomalous pulmonary venous drainage, the incidence of which has been much higher than that previously reported. We have observed that the most severe malformations are preferably found in 45,X, while the ring pattern is characterized by a very high incidence of bicuspid aorta. No anomaly was found in the patients with X isochromosome.

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