[6岁前特纳氏综合征女孩的自发生长]。

Andrzej Wiśniewski, Katarzyna Milde, Romuald Stupnicki
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引用次数: 0

摘要

背景:特纳氏综合征(TS)是最常见的遗传性疾病之一,其发病率为每1900-2500例活产女婴中有一例。明显的身材矮小是该病的主要症状,未经治疗的妇女成年后的平均身高比健康妇女低23厘米。根据Ranke的说法,发育障碍早在胎儿时期就出现了,并且导致了与胎龄有关的出生时身体长度和质量缺陷。目的:修正目前关于TS女孩身体发育过程的观点,特别是在婴儿期和幼儿期。材料与方法:对474例特纳氏综合征女性新生儿进行研究,以二次妊娠居多,不少于38周。染色体分析证实了特纳氏综合征。出生时体重(BM)与Usher和McLean设计的胎龄标准(GA)有关。结果:TS从婴儿期开始出现生长障碍,2 ~ 3岁的生长速度与健康人群相似。然而,在这段时间之后,特纳女孩的生长速度稳步下降,正如TS的百分位数标准所显示的那样。在6岁时,特纳女孩与健康女孩之间的平均身高差异超过了未经治疗的成年TS女性最终生长缺陷的1/3。结论:我们已经证明,特纳新生儿的体重和长度与胎龄有关是正常的。只有约5%的新生儿同时出现身高和体重缺陷超过-2 SD,这种缺陷归因于宫内生长迟缓(IUGR)。在临床实践中,新生儿没有记录的胎儿生长速度下降,但有明显的体长缺陷,被诊断为iugr折磨。由于我们的新生儿很少同时出现体长和质量缺陷,因此IUGR被认为不太可能导致特纳女孩的生长缺陷。在大约1/5的特纳新生儿中发现体重或长度不足(分别为19%和1%)。由于这些缺陷中的任何一种都表明子宫内营养不良(胎龄较小,SGA),后者应被认为在TS中比在一般人群中更常见。因此,SGA似乎是TS的症状之一,因此在解释女性新生儿的体重和/或身高缺陷时应予以考虑。具有典型TS染色体畸变的胎儿的生长障碍,在所有可能性中,与具有正常x染色体的胎儿一样频繁。
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[Spontaneous growth of girls with Turner's syndrome until 6 years of age].

Background: Turner's syndrome (TS) is one of the most common genetically conditioned diseases, its incidence amounting to one per 1900-2500 live female births. A marked short stature is a prime symptom of the disease, the average adult body height of untreated women being by 23 cm lower than that of healthy ones. According to Ranke, developmental disorders appear as early as in foetal life and are responsible for body length and mass deficits at birth in relation to gestational age.

Objectives: To revise present views regarding the course of physical development of girls with TS, especially at infancy and early childhood.

Material and methods: A total of 474 female newborns with Turner's syndrome were studied, the pregnancies, mostly second ones, not less than 38 weeks. Turner's syndrome was confirmed by chromosome analysis. Body mass at birth (BM) was related to the norms for gestational age (GA) designed by Usher and McLean.

Results: Growth disorders take place in TS since infancy, the growth rates in the age period of 2-3 years being similar to those observed in healthy population. After that period, however, growth rate in Turner girls steadily decreases as shown in percentile norms for TS. At the age of 6 years, the average difference in body height between Turner and healthy girls exceeds 1/3 of the final growth deficit noted in untreated adult women with TS.

Conclusion: We have demonstrated that body mass and length of Turner newborns were normal in relation to gestational age. Only in about 5% of newborns a simultaneous length and weight deficit exceeded -2 SD, and that deficit was attributed to intrauterine growth retardation (IUGR). In clinical practice, newborns without documented decrease in foetal growth rate, but having a pronounced body length deficit, are diagnosed as IUGR-afflicted. Since simultaneous body length and mass deficits were rare in our newborns, IUGR was regarded as unlikely in bringing about growth deficit in Turner girls. In about 1/5 of Turner newborns a weight or length deficit was found (19 and 1%, respectively). Since either of those deficits evidences intrauterine dystrophy (small for gestational age, SGA), the latter one should be considered much more frequent in TS than in the general population. Therefore, SGA appears to be one of the symptoms of TS and should thus be taken into account when explaining body mass and/or length deficit in female newborns. Growth disorders in foetuses with chromosomal aberrations typical of TS are, in all probability, as frequent as in those with normal both X-chromosomes.

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