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21号染色体部分三体。进一步证明21q22带的三体对于唐氏综合征表型至关重要。

Partial trisomy 21. Further evidence that trisomy of band 21q22 is essential for Down's phenotype.

作者信息

Hagemeijer A, Smit E M

出版信息

Hum Genet. 1977 Aug 31;38(1):15-23. doi: 10.1007/BF00295803.

Abstract

Cytogenetic analysis of a 6-year-old girl with moderate mental retardation revealed 46 chromosomes with a tandem translocation (21;21) resulting in a partial trisomy 21. Only the terminal band 21q22 was not in triplicate. G-, Q-, R-, and C-banding techniques and silver nitrate staining of the nucleolus organizer regions (NORs) were used to identify this chromosome fully. The phenotype of the patient was not typical for Down's syndrome, providing additional evidence that trisomy of band 21q22 is pathogenetic for the phenotype of Down's syndrome. This is also a new example in human pathology of a stable 'dicentric' chromosome in which one of the centromeric constrictions appears to be nonfunctional.

摘要

对一名患有中度智力发育迟缓的6岁女孩进行细胞遗传学分析,结果显示其有46条染色体,存在串联易位(21;21),导致21号染色体部分三体。只有末端带21q22不是三倍体。采用G显带、Q显带、R显带和C显带技术以及核仁组织区(NORs)的硝酸银染色对该染色体进行全面鉴定。该患者的表型并非典型的唐氏综合征,这进一步证明21q22带的三体性是唐氏综合征表型的致病原因。这也是人类病理学中一个稳定的“双着丝粒”染色体的新例子,其中一个着丝粒缢痕似乎无功能。

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