Ergür Ayça T, Ocal Gönül, Berberoglu Merih, Tekin Mustafa, Kiliç Birim G, Aycan Zehra, Kutlu Alev, Adiyaman Pelin, Siklar Zeynep, Akar Nejat, Sahin Aynur, Akçayöz Duygu
Division of Pediatric Endocrinology, Faculty of Medicine, Ankara University, Ankara, Turkey.
Pediatr Int. 2008 Apr;50(2):172-4. doi: 10.1111/j.1442-200X.2008.02540.x.
45,X Turner syndrome (TS) female subjects have visuospatial skill and social cognition deficits that may arise from X-linked imprinting. The aim of the present study was to compare phenotypic characteristics and neurocognitive pattern of 12 monosomic TS girls, according to X-linked imprinting.
Microsatellite markers were used to determine the parental origin of the missing chromosome X. Wechsler Intelligence Scale for Children-Revised (WISC-R) was administered as measures of general intellectual functioning. The results were compared in TS patients with maternally derived X chromosome (Xm) and paternally derived X chromosome (Xp).
Six out of 12 patients (50%) had Xm, and the other six (50%) had Xp chromosome. There was no difference in the total, verbal and performance IQ score between the TS subgroups with Xm and Xp. When the WISC-R subtest score patterns were compared, the mean arithmetic scores were significantly poorer in the Xm TS than in the Xp TS.
In monosomic TS cases, paternal imprinting may predict arithmetic ability, on the other hand, reductionist consideration defined by genetic imprinting is not sufficient to confirm this. Further studies should be undertaken to clarify this situation.
45,X特纳综合征(TS)女性患者存在视觉空间技能和社会认知缺陷,这些缺陷可能源于X连锁印记。本研究的目的是根据X连锁印记比较12名单体性TS女孩的表型特征和神经认知模式。
使用微卫星标记来确定缺失的X染色体的亲本来源。使用韦氏儿童智力量表修订版(WISC-R)作为一般智力功能的测量工具。将患有母源X染色体(Xm)和父源X染色体(Xp)的TS患者的结果进行比较。
12名患者中有6名(50%)具有Xm,另外6名(50%)具有Xp染色体。具有Xm和Xp的TS亚组之间的总智商、语言智商和操作智商得分没有差异。当比较WISC-R子测试得分模式时,Xm TS的平均算术得分显著低于Xp TS。
在单体性TS病例中,父源印记可能预测算术能力,另一方面,由基因印记定义的简化主义考虑不足以证实这一点。应进行进一步研究以阐明这种情况。