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特纳综合征中单一X染色体的亲本来源:与亲本年龄或临床表型无关。

The parental origin of the single X chromosome in Turner syndrome: lack of correlation with parental age or clinical phenotype.

作者信息

Mathur A, Stekol L, Schatz D, MacLaren N K, Scott M L, Lippe B

机构信息

Department of Pediatrics, University of California School of Medicine, Los Angeles.

出版信息

Am J Hum Genet. 1991 Apr;48(4):682-6.

Abstract

We have used X- and Y-linked RFLPs to determine the origin of the single X chromosome in 25 live-born individuals with Turner syndrome. We determined that 18 individuals retained a maternal X (Xm) and that seven retained the paternal X (Xp). No occult mosaicism was detected. We found no differences in either maternal or paternal ages for the two groups. The ratio of maternal X to paternal X is just over 2:1, which is consistent with the expected proportion of meiotic or mitotic products, with equal loss at each step, given the nonviability of 45,Y. Six phenotypic or physiologic characteristics were assessed: (1) birth weight, (2) height percentile at time of testing, (3) presence of a webbed neck, (4) cardiovascular abnormalities, (5) renal abnormalities, and (6) thyroid autoimmunity. There were no significant differences in birth weights or heights between the girls who retained the maternal X or the paternal X. In addition, no differences between the groups could be appreciated in the incidence of the physical, anatomic, or physiologic parameters assessed.

摘要

我们利用X连锁和Y连锁限制性片段长度多态性(RFLPs)来确定25例活产特纳综合征患者单一X染色体的来源。我们确定18例个体保留了母源X染色体(Xm),7例保留了父源X染色体(Xp)。未检测到隐匿性嵌合体。我们发现两组的母龄或父龄均无差异。母源X与父源X的比例略高于2:1,这与减数分裂或有丝分裂产物的预期比例一致,考虑到45,Y个体无法存活,在每个步骤中损失相等。评估了六个表型或生理特征:(1)出生体重,(2)检测时的身高百分位数,(3)蹼颈的存在,(4)心血管异常,(5)肾脏异常,以及(6)甲状腺自身免疫。保留母源X或父源X的女孩在出生体重或身高方面无显著差异。此外,在评估的身体、解剖或生理参数的发生率上,两组之间也没有差异。

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