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[染色体断裂综合征与脆性X综合征]

[Chromosome breakage syndrome and fragile X syndrome].

作者信息

Shiraishi Y

机构信息

First Department of Anatomy, Kochi Medical School.

出版信息

Nihon Rinsho. 1995 Nov;53(11):2807-14.

PMID:8538049
Abstract

Chromosome instability is a characteristic cytogenetic feature of a number of genetically determined human disorders collectively known as chromosome breakage syndromes. Included among the disorders are Bloom's syndrome (BS), Fanconi's anemia (FA), ataxia telangiectasia (AT). In each of the syndromes chromosome instability exists in the form of increased frequencies of breaks and interchanges occurring either spontaneously or following treatment with various DNA-damaging agents. These diseases have in common an autosomal recessive transmission and an increased tendency to develop malignancies. The blood cells of subjects with AT, BS, or FA are significantly more radiosensitive than those of controls, particularly in the occurrence of chromosome aberrations.

摘要

染色体不稳定性是许多遗传决定的人类疾病的一个特征性细胞遗传学特征,这些疾病统称为染色体断裂综合征。其中包括布卢姆综合征(BS)、范科尼贫血(FA)、共济失调毛细血管扩张症(AT)。在每种综合征中,染色体不稳定性以自发或在使用各种DNA损伤剂处理后断裂和互换频率增加的形式存在。这些疾病的共同特点是常染色体隐性遗传和发生恶性肿瘤的倾向增加。患有AT、BS或FA的受试者的血细胞比对照组的血细胞对辐射更敏感,尤其是在染色体畸变的发生方面。

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