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| 21-三体综合征标准型1例 | |
| 引用本文： | 张榴榴,张沛中. 21-三体综合征标准型1例[J]. 安徽卫生职业技术学院学报, 2014, 0(5): 111-112 |
| 作者姓名： | 张榴榴 张沛中 |
| 作者单位： | 1. 安徽省妇幼保健院普儿科 安徽 230001 2. 阜阳卫生学校 安徽 236015 |
| 摘 要： | 21-三体综合征（唐氏综合征、先天愚型、伸舌样综合征）是发现最早的染色体数目畸变引起的染色体病，临床较常见。该文报告标准型患儿1例，并结合临床实践对该病在诊断、治疗、再发风险、预防及预后等方面进行讨论。 |
| 关 键 词： | 21-三体综合征 染色体 核型诊断 感染治疗 |
A report and discussion of Trisomy 21 |
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| ZHANGLiu-liu,ZHANGPei-zhong. A report and discussion of Trisomy 21[J]. Journal of Anhui Heaith Vocational & Technical College, 2014, 0(5): 111-112 | |
| Authors: | ZHANGLiu-liu ZHANGPei-zhong |
| Affiliation: | ZHANG Liu-liu, ZHANG Pei-zhong( 1.Anhui Province-Maternal and Child Health Hospital, Hefei 230001, Anhui) |
| Abstract: | Trisomy 21 （Down syndrome,Down＇s syndrome,Tongue syndrome）is typically found in the earliest change the number of deformities caused by chromosomal disease which is a disease in clinical comparison. This re- port explains the children with standard disease and combines with the clinical practice to make discussion in the di- agnosis, treatment,recurrence risks,prevention and prognosis. |
| Keywords: | Trisomy21 Karyotype Diagnosis Geneticcounseling |
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