Mazzanti L, Prandstraller D, Tassinari D, Rubino I, Santucci S, Picchio F M, Forabosco A, Cacciari E
2nd Pediatric Clinic, University of Bologna, Italy.
Helv Paediatr Acta. 1988 Aug;43(1-2):25-31.
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.
55例具有不同核型的特纳综合征患者接受了全面的心脏评估(体格检查、心电图、胸部X线和超声心动图)。发现先天性心脏病的发生率为17%。与普通人群相比,仅主动脉缩窄和部分肺静脉异位引流的发生率显著更高(p<0.001)。在特纳综合征患者的心脏异常中,主动脉畸形(主动脉缩窄、主动脉狭窄、二叶主动脉)最为常见,其次是部分肺静脉异位引流,其发生率远高于先前报道。我们观察到,最严重的畸形多见于45,X核型患者,而环状核型的特征是二叶主动脉发生率非常高。等臂X染色体患者未发现异常。