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Updated: May 17, 2025

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Chromosome Preparation From Cultured Cells
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[21号环染色体综合征:2例病例报告]
Tania Alejandra Guzmán-Santiago1, Daniela Juárez-Melchor1, Berenice Jiménez-Pérez1
1Instituto Mexicano del Seguro Social, Hospital General de Zona No. 20 "La Margarita", Servicio de Genética Médica. Puebla, Puebla, México.
Revista medica del Instituto Mexicano del Seguro Social
|April 23, 2025
概括
环21综合征,以轻微的异形和发育迟缓为特征,在两名男性患者中呈现. 本案例研究突出了与这种罕见的染色体异常相关的关键临床特征.
科学领域:
- 遗传学 是一个遗传学.
- 人类遗传学 人类遗传学
- 染色体异常 染色体异常
背景情况:
- 环染色体是当染色体有两个断裂,断裂的末端连接时形成的.
- 21环综合征表现为轻微的形状变异,血栓细胞减少,以及精神运动和语言延迟.
研究的目的:
- 介绍两名被诊断为21号环染色体的男性患者.
主要方法:
- 两名男性患者的病例报告.
- 型鉴定以确认21号环染色体的存在.
主要成果:
- 患者1:一个5岁的男性,精神运动和语言延迟,表现出面异形,包括突出的美托皮和表角. 型: 46,XY,r(21)) p11.2q21). 型: 46,XY,r(21) p11.2q21). 型: 46,XY,r(21) p11.2q21). 型: 46,XY,r(21) p11.2q21). 型: 46,XY. 型: 46,XY. 型: 46,XY. 型: 46,XY.
- 患者2:8岁的男性精神运动和语言延迟,呈现出平的头,三角形的面孔和低落的耳朵. 型:46,XY,r(21)(p11q22). 这种型的
结论:
- 面异形和精神运动/语言延迟是21环染色体综合征的显著临床表现.
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