男性唐氏综合症的皮肤纹评估

R. Parveen, M. Rahman, Mahmud Ahmed, Md. Ashraful Azim, Zeenatul Momena, Mohammad Nahid Salman
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引用次数: 0

摘要

唐氏综合症(DS)是最常见的导致智力残疾的染色体疾病。这主要是由于21号染色体存在额外的拷贝。皮肤印记已被很好地确立为许多具有遗传基础的疾病的诊断援助。皮纹数据是通过在纸上使用墨水和印刷品获得的。这项横断面分析型研究于2017年1月至2017年12月在达卡医学院解剖学系对40名唐氏综合征受试者(年龄从6岁到16岁不等)进行了研究,这些受试者分别来自孟加拉国智障人士福利协会(SWID, Bangladesh)和孟加拉国唐氏综合征协会(DSS),并与40名对照组进行了比较,以建立两组之间的比较。采用皮纹印评价对照与DS个体在“atd”、“data”、“adt”角度和图案强度上的差异。结果表明,唐氏雄性的“atd”角显著高于对照组(p<0.05)。指型学研究还显示,唐氏综合征组双手的“数据”“adt”角度(p<0.05)和模式强度(p<0.001)较低。该方法无创且成本有效。观察到的“atd”、“dat”和“adt”角度的变化加上纹纹研究的模式强度证明,这种简单的技术可以作为选择DS个体进行细胞遗传学分析的有价值的工具。《中国医学杂志》2022年7月第11期[02:44 . 151
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dermatoglyphic Assessment in Male Down Syndrome
Down syndrome (DS) is the most common chromosomal disorder which causes intellectual disability. It is mainly because of the presence of extra copy of chromosome number 21. Dermatoglyphic has been well established as a diagnostic aid in number of diseases having hereditary basis. Dermatoglyphic data was obtained by the use of ink and prints on a paper. This cross-sectional, analytical type of study was performed at the Department of Anatomy, Dhaka Medical College, Dhaka from January 2017 to December 2017 on 40 Down syndrome subjects (age ranged from 6 to 16) selected from Society for the Welfare of the Intellectually Disabled, Bangladesh (SWID, Bangladesh) and Down Syndrome Society of Bangladesh (DSS) and compared with 40 controls for the establishment of comparison between two groups. Dermatoglyphic prints were used to evaluate the difference in „atd‟ „dat‟ „adt‟ angles and pattern intensity between the control and the DS individuals. The results showed that „atd‟ angle was significantly higher (p<0.05) in Down males than the controls. The dactylography study also revealed lower „dat‟ „adt‟ angles (p<0.05) and pattern intensity (p<0.001) in both hands of Down syndrome group. This method is non-invasive and cost effective. The observed changes in the „atd‟ „dat‟ and „adt‟ angles plus the patterns intensity in the dermatoglyphic study proved that this simple technique could be a valuable tool for selecting individuals of DS for cytogenetic analysis. CBMJ 2022 July: vol. 11 no. 02 P: 144-151
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