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[部分三体综合征的遗传学。I. 2q三体]

[Genetics of partial trisomies. I. Trisomy 2q].

作者信息

Lur'e I V, Rumiantseva N V, Podleshchuk L V, Kaurov B A, Zaletaev D V

出版信息

Genetika. 1986 Jun;22(6):1033-9.

PMID:3732802
Abstract

The family, where 2 children had partial trisomy 2q33-q ter, due to paternal translocation t(2;18) (q33;p11.1), was examined. The analysis of 36 cases of trisomy 2q showed that the forms connected with parental chromosomal rearrangement prevailed in the genesis of trisomy 2q. Moreover, the balanced carrier-mothers were more common than fathers. The 2q34-q ter segment may be considered "critical" for occurrence of trisomy 2q syndrome. In case of equal triplication, the similarity between the patients within the same family is greater than between those from different families. The value of intragroup similarity between the patients with equal trisomies may be used for evaluation of phenotypical similarity at different triplicated segments.

摘要

对一个家庭进行了检查,该家庭中有2名儿童因父亲的t(2;18)(q33;p11.1)易位而患有2q33-q末端部分三体。对36例2q三体病例的分析表明,与亲代染色体重排相关的类型在2q三体的发生中占主导地位。此外,平衡携带者母亲比父亲更常见。2q34-q末端片段可能被认为是2q三体综合征发生的“关键”片段。在均等三体的情况下,同一家族内患者之间的相似性大于不同家族患者之间的相似性。均等三体患者组内相似性的值可用于评估不同重复片段处的表型相似性。

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