遗传 ›› 2003, Vol. 25 ›› Issue (4): 396-396.

• 论文 • 上一篇    下一篇

新生儿缺氧性脑病伴46,XX,-21,+t(21;21)罕见核型一例

付建华1;宁建英2;张青1;付睿婷1;李露霞1 FU Jian-Hua1;NING Jian-Ying2;ZHANG Qing1;FU Rui-Ting1;LI Lu-Xia1   

  1. 1.新疆石河子大学医学院,石河子 832002; 2.新疆石河子大学医学院第一附属医院,石河子 832002 1.School of Medicine,Shihezi University, Shihezi 832002,China; 2.The First Affiliated Hospital, School of Medicine ,Shihezi University,Shihezi 832002, China
  • 收稿日期:1900-01-01 出版日期:2003-08-10 发布日期:2003-08-10

A Newborn Case of Hypoxic-Ischemic Encephalopathy Accompanied with 46,XX,-21,+t(21;21)

  • Received:1900-01-01 Online:2003-08-10 Published:2003-08-10

摘要: Abstract:This report describes a cytogenetic aberration in one neonatal patient with hypoxic-ischemic encephalopathy.A rare karyotype,46,XX,-21,+t(21;21), was detected.This de nono chromosomal abnormality may be caused by the meiotic non-disjunction of chromosomes during gametogenesis along with the formation of Robertsonian translocation between homologous chromosome 21.

关键词: 多菌灵, 玉蜀黍赤霉, 遗传, 抗药突变体, chromosome abnormality, hypoxic-ischemic encephalopathy,
Key words,
neonate

Key words: Gibberella zeae, carbendazim, genetics, resistant mutants