Tan K B L, Yeo G S H
Clinical Research Centre, Yong Loo Lin School of Medicine, National University of Singapore, Block MD11, #02-02, 10 Medical Drive, Singapore.
Singapore Med J. 2009 Jun;50(6):587-90.
Turner syndrome is the most common sex chromosomal abnormality in female foetuses, and is associated with a high proportion of cardiac anomalies. The aim of this study was to look at the incidence, demographical data and epidemiological pattern of Turner syndrome in Singapore from 1999 to 2004 and to examine the birth defects associated with this condition, specifically with reference to cardiac defects.
Data on Turner syndrome cases born in 1999-2004 were retrieved from the National Birth Defects Registry (NBDR) and analysed. Data on congenital cardiac defect cases notified to the NBDR in the same time period were also retrieved and compared with the Turner syndrome cases.
There were a total of 101 cases of Turner syndrome in the six-year period from 1999-2004, yielding an overall incidence of 0.85 per 1,000 female live births, or one in 1,180 female live births. The incidence was lowest among Indians (0.38 per 1,000) compared to Malays (0.72 per 1,000) and Chinese (0.90 per 1,000). 75 cases (74.3 percent) had the 45,X karyotype, while the other 26 cases (25.7 percent) were mosaics. The mean maternal age for 45,X was lower (32.2 years, range 22-42) compared to mosaics (34.5 years, range 27-40). 19.8 percent (20/101) were live births, 38.6 percent (39/101) were terminated pregnancies and 41.6 percent (42/101) were spontaneous miscarriages. 13.9 percent of Turner syndrome babies had cardiac defects compared to 1.2 percent in the general population (p-value is less than 0.0001). Major cardiac defects found among Turner syndrome babies compared to the general population included the coarctation of the aorta (5.9 percent compared to 0.03 percent, p-value is less than 0.0001), atrial septal defects (3.0 percent compared to 0.6 percent, p-value is 0.006), a hypoplastic left heart (2.0 percent compared to 0.05 percent, p-value is less than 0.0001), aortic hypoplasia (3.0 percent compared to 0.01 percent, p-value is less than 0.0001) and dextrocardia (1.0 percent compared to 0.02 percent, p-value is 0.0002).
Cardiac defects, particularly left-sided ones, are significantly more common among Turner syndrome foetuses. The true incidence of this syndrome is likely to be higher than that quoted in this study, and can only be solved when a complete screening of an entire population has been performed.
特纳综合征是女性胎儿中最常见的性染色体异常疾病,且与高比例的心脏畸形有关。本研究的目的是观察1999年至2004年新加坡特纳综合征的发病率、人口统计学数据和流行病学模式,并研究与该疾病相关的出生缺陷,特别是心脏缺陷。
从国家出生缺陷登记处(NBDR)检索并分析1999 - 2004年出生的特纳综合征病例数据。同时检索同一时期向NBDR报告的先天性心脏缺陷病例数据,并与特纳综合征病例进行比较。
1999年至2004年的六年期间,共有101例特纳综合征病例,总发病率为每1000例女性活产中有0.85例,即每1180例女性活产中有1例。印度人的发病率最低(每1000例中有0.38例),而马来人(每1000例中有0.72例)和中国人(每1000例中有0.90例)的发病率较高。75例(74.3%)具有45,X核型,另外26例(25.7%)为嵌合体。45,X患者的母亲平均年龄较低(32.2岁,范围22 - 42岁),而嵌合体患者的母亲平均年龄为34.5岁(范围27 - 40岁)。19.8%(20/101)为活产,38.6%(39/101)为终止妊娠,41.6%(42/101)为自然流产。13.9%的特纳综合征婴儿有心脏缺陷,而普通人群中的这一比例为1.2%(p值小于0.0001)。与普通人群相比,特纳综合征婴儿中发现的主要心脏缺陷包括主动脉缩窄(5.9% 对比0.03%,p值小于0.0001)、房间隔缺损(3.0% 对比0.6%,p值为0.006)、左心发育不全(2.0% 对比0.05%,p值小于0.0001)、主动脉发育不全(3.0% 对比0.01%,p值小于0.0001)和右位心(1.0% 对比0.02%,p值为0.0002)。
心脏缺陷,尤其是左侧心脏缺陷,在特纳综合征胎儿中明显更为常见。该综合征的实际发病率可能高于本研究中引用的数字,只有在对整个人口进行全面筛查后才能得出准确结果。