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Autosomal Trisomies and Partial Trisomy Syndromes: (With Presentation of Two Cases of Partial Trisomy for the E Group of Chromosomes)

机译:常染色体三体性和部分三体综合症:(附有两例E染色体组的部分三体性病例)

摘要

The establishing of 46 chromosomes as the normal complement in man and the report of the sex chromatin bodies in buccal smears were followed by reports of trisomies and other abnormal patterns of the X and Y chromosomes in Klinefelter's and Turner's syndromes. Abnormal autosomal complements were described in mongolism, in the E-trisomy syndrome, the D-trisomy syndrome, in the Sturge-Weber syndrome, Waldenstrom's macroglobulinemia, benign congenital hypotonia, atrial septal defect and in the schizoid personality. Certain of these conditions, as well as the “oral-facial-digital” syndrome, were also found to exist as partial trisomies. The mechanism of a trisomy is one of non-disjunction and of partial trisomy translocation or insertion. Two cases of the partial trisomy in the E group are described; these are of especial interest because of the familial incidence, longer survival and male sex occurrence, features which are rarely seen in the full E-trisomy syndrome.
机译:建立了46条染色体作为人类的正常补体,并在颊部涂片中出现了性染色质体的报道,随后报道了Klinefelter和Turner综合征的三体性以及X和Y染色体的其他异常模式。常态补体异常在蒙古族,E-三体综合征,D-三体综合征,Sturge-Weber综合征,Waldenstrom巨球蛋白血症,良性先天性肌张力低下,房间隔缺损和精神分裂症人格中都有描述。还发现其中某些情况以及“口-面-数字”综合症也存在部分三体性。三体性的机制是不分离和部分三体性易位或插入的一种。描述了E组中的部分三体性的两种情况。由于家族性发病率,更长的生存期和男性发生率,这些都是特别令人感兴趣的,而这些特征在完整的E-三体综合征中很少见。

著录项

  • 作者

    Zaleski W. A.;

  • 作者单位
  • 年度 100
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  • 原文格式 PDF
  • 正文语种 eng
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