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[Identification of causal relationship between fibrous dysplasia of fibula and fracture: A case report]. [腓骨纤维发育不良与骨折因果关系的鉴定:1例报告]。
Pub Date : 2023-10-25 DOI: 10.12116/j.issn.1004-5619.2022.220807
琨 朱, 东 高, 利 华 范
李某,男,28岁,某年12月6日在篮球比赛中右小腿与他人碰撞后倒地,临床诊断为右腓骨病理性骨折。现委托单位要求对本次外伤与李某右腓骨病理性骨折之间的因果关系及参与程度进行法医临床鉴定。.
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引用次数: 0
Research Progress on Molecular Biology of Human Height Estimation. 人体身高估算的分子生物学研究进展。
Pub Date : 2023-10-25 DOI: 10.12116/j.issn.1004-5619.2022.520301
Zhong-Hua Wang, Shu-Jin Li

As an important anthropometric characteristic, human height not only contributes to the recognition of other anthropological characteristics and genetic risk factors, but also is an important part of forensic DNA phenotyping studies. Accurate estimation of height can provide more complete information about the phenotype of suspects and provide help to solve cases. In recent years, having benefited from the rapid development of molecular biological techniques and bioinformatics, height-related genetics research has made some progress. This paper describes the research progress of human height estimation from the genetic variation and the epigenetic inheritance perspectives and looks into the future research direction.

身高作为一项重要的人体测量特征,不仅有助于识别其他人类学特征和遗传危险因素,而且是法医DNA表型研究的重要组成部分。准确的身高估计可以提供更完整的嫌疑人表型信息,为破案提供帮助。近年来,得益于分子生物学技术和生物信息学的快速发展,身高相关遗传学研究取得了一定进展。本文从遗传变异和表观遗传两方面介绍了人类身高估算的研究进展,并展望了未来的研究方向。
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引用次数: 0
[Assessing the disability of enophthalmos with CT scanning measurement method: A case report]. [用CT扫描测量法评价眼球内陷的致残性:1例报告]。
Pub Date : 2023-10-25 DOI: 10.12116/j.issn.1004-5619.2021.210905
强 李, 志 浩 付, 晓 东 孙, 效 宇 黄
王某,女,46岁,某年7月28日因“左眼部及左颜面部外伤后4 h”入院治疗。伤后当日CT检查提示:左眼眶内侧壁、顶壁、下壁及左侧筛窦筛板骨折,左侧上颌骨额突骨折,左侧中切牙部分缺损,左侧侧切牙根折,左侧内直肌、上直肌、下直肌挫伤,左眼眶肌锥内间隙少许渗出,左侧上颌窦、筛窦及额窦积血,左侧颌面部及眶周软组织肿胀。查体:睁眼受限,视力、眼压未查。左眼部及颜面部青紫、肿胀,左眼外眦部可见约3 cm裂伤,余检查无法进行;右眼正常。临床诊断为左眼眶骨折、左眼球挫伤、上颌骨骨折、外伤性牙折断、左眼视网膜出血。予清创缝合、左眼眶骨折整复手术(钛网植入)、止血药物、营养神经、局部抗生素等对症治疗后出院。出院后多次以左眼球内陷、视物重影为主诉眼科门诊随诊,同年9月29日及次年3月17日查眼球突出度:右侧19 mm、左侧16 mm(眶距105 mm),右侧19 mm、左侧15 mm(眶距105 mm)。现委托对王某的残疾程度进行评定。.
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引用次数: 0
[Discussion on the cause of secondary traffic injury: A case report]. 【二次交通伤害成因探讨:1例报告】。
Pub Date : 2023-10-25 DOI: 10.12116/j.issn.1004-5619.2022.220613
丹 丹 林, 莉 莉 赵, 芳 芳 施, 雅 婷 陈, 国 南 潘
被鉴定人,男,35岁,某年10月26日03:50,驾驶轻型厢式货车碰撞道路中央绿化带及路灯后受伤,具体伤情不详。同日04:15,该男在被救护车送医途中又遭遇车辆追尾交通事故。被鉴定人诉在救护车追尾事故中,未从救护车内的担架上摔下来,但救护车内仪器设备掉落砸伤左下肢,具体砸伤部位不明。法院委托要求对第二次交通事故能否造成被鉴定人左下肢损伤进行鉴定。.
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引用次数: 0
Cross-Platform Application of DNA Methylation Age Estimation Model in Eastern Chinese Han Population. DNA甲基化年龄估计模型在中国东部汉族人群中的跨平台应用
Pub Date : 2023-10-25 DOI: 10.12116/j.issn.1004-5619.2022.520405
Zi-Wei Wang, Cheng-Tao Li, Xi-Ling Liu

Objectives: To evaluate the forensic application value of an age estimation model based on DNA methylation in eastern Chinese Han population, and to provide a theoretical basis for exploring age estimation models suitable for different detection platforms.

Methods: According to the 6 age-related methylation sites in the published blood DNA methylation age estimation models of Chinese Han population, the DNA methylation level of 48 samples was detected by pyrosequencing and next-generation sequencing (NGS). After submitting DNA methylation levels to the age estimation model, the DNA methylation ages were predicted and compared with their real ages.

Results: The 6 DNA methylation sites in both detection techniques were age-related, with an R2 of 0.85 and a median absolute deviation (MAD) of 4.81 years when using pyrosequencing;with an R2 of 0.84 and MAD of 4.41 years when using NGS.

Conclusions: The blood DNA methylation age estimation model can be used under pyrosequencing and multi-purpose regional methylation enrichment sequencing technology based on NGS and it can accurately estimate the age.

目的:评价基于DNA甲基化的中国东部汉族人群年龄估计模型的法医应用价值,为探索适合不同检测平台的年龄估计模型提供理论依据。方法:根据已发表的中国汉族人群血液DNA甲基化年龄估计模型中6个与年龄相关的甲基化位点,采用焦磷酸测序和下一代测序(NGS)检测48份样本的DNA甲基化水平。将DNA甲基化水平提交给年龄估计模型后,预测DNA甲基化年龄并将其与实际年龄进行比较。结果:两种检测技术的6个DNA甲基化位点均与年龄相关,使用焦磷酸测序时,R2为0.85,中位绝对偏差(MAD)为4.81年;使用NGS时,R2为0.84,MAD为4.41年。结论:基于NGS的焦磷酸测序和多用途区域甲基化富集测序技术下的血液DNA甲基化年龄估计模型能够准确估计年龄。
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引用次数: 0
Qualitative and Quantitative Analysis of Five Indoles or Indazole Amide Synthetic Cannabinoids in Suspected E-Cigarette Oil by GC-MS. 气相色谱-质谱联用分析疑似电子烟油中5种吲哚或吲哚酰胺类合成大麻素。
Pub Date : 2023-10-25 DOI: 10.12116/j.issn.1004-5619.2022.320101
Cui-Mei Liu, Wei Jia, Chun-Hui Song, Zhen-Hua Qian, Zhen-Dong Hua, Yue-Meng Chen

Objectives: To establish the GC-MS qualitative and quantitative analysis methods for the synthetic cannabinoids, its main matrix and additives in suspicious electronic cigarette (e-cigarette) oil samples.

Methods: The e-cigarette oil samples were analyzed by GC-MS after diluted with methanol. Synthetic cannabinoids, its main matrix and additives in e-cigarette oil samples were qualitatively analyzed by the characteristic fragment ions and retention time. The synthetic cannabinoids were quantitatively analyzed by using the selective ion monitoring mode.

Results: The linear range of each compound in GC-MS quantitative method was 0.025-1 mg/mL, the matrix recovery rate was 94%-103%, the intra-day precision relative standard deviations (RSD) was less than 2.5%, and inter-day precision RSD was less than 4.0%. Five indoles or indazole amide synthetic cannabinoids were detected in 25 e-cigarette samples. The main matrixes of e-cigarette samples were propylene glycol and glycerol. Additives such as N,2,3-trimethyl-2-isopropyl butanamide (WS-23), glycerol triacetate and nicotine were detected in some samples. The content range of synthetic cannabinoids in 25 e-cigarette samples was 0.05%-2.74%.

Conclusions: The GC-MS method for synthesizing cannabinoid, matrix and additive in e-cigarette oil samples has good selectivity, high resolution, low detection limit, and can be used for simultaneous qualitative and quantitative analysis of multiple components; The explored fragment ion fragmentation mechanism of the electron bombardment ion source of indole or indoxamide compounds helps to identify such substances or other compounds with similar structures in cases.

目的:建立可疑电子烟(电子烟)油样品中合成大麻素及其主要基质和添加剂的气相色谱-质谱联用定性和定量分析方法。方法:采用甲醇稀释后的气相色谱-质谱法对电子烟油样品进行分析。通过特征碎片离子和保留时间对电子烟油样品中的合成大麻素及其主要基质和添加剂进行定性分析。采用选择性离子监测模式对合成大麻素进行定量分析。结果:各化合物在GC-MS定量方法中线性范围为0.025 ~ 1 mg/mL,基质回收率为94% ~ 103%,日内精密度相对标准偏差(RSD) < 2.5%,日内精密度RSD < 4.0%。在25份电子烟样品中检出5种吲哚类或吲哚胺类合成大麻素。电子烟样品的主要基质为丙二醇和甘油。在部分样品中检测到N,2,3-三甲基-2-异丙基丁酰胺(WS-23)、三乙酸甘油和尼古丁等添加剂。25份电子烟样品中合成大麻素的含量范围为0.05% ~ 2.74%。结论:采用气相色谱-质谱法合成电子烟油样品中的大麻素、基质和添加剂,选择性好,分辨率高,检出限低,可同时对多组分进行定性和定量分析;所探索的吲哚或吲哚酰胺类化合物的电子轰击离子源的碎片离子碎裂机制,有助于在某些情况下识别这类物质或具有类似结构的其他化合物。
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引用次数: 0
Research Progress and Forensic Application of Human Vascular Finite Element Modeling and Biomechanics. 人体血管有限元建模与生物力学研究进展及法医应用。
Pub Date : 2023-10-25 DOI: 10.12116/j.issn.1004-5619.2021.411103
Yong Zeng, Dong-Hua Zou, Ying Fan, Qing Xu, Lu-Yang Tao, Yi-Jiu Chen, Zheng-Dong Li

The finite element method (FEM) is a mathematical method for obtaining approximate solutions to a wide variety of engineering problems. With the development of computer technology, it is gradually applied to the study of biomechanics of human body. The application of the combination of FEM and biomechanics in exploring the relationship between vascular injury and disease, and pathological mechanisms will be a technological innovation for traditional forensic medicine. This paper reviews the construction and development of human vascular FEM modeling, and its research progress on the vascular biomechanics. This paper also looks to the application prospects of FEM modeling in forensic pathology.

有限元法(FEM)是一种获得各种工程问题近似解的数学方法。随着计算机技术的发展,它逐渐被应用到人体生物力学的研究中。将有限元法与生物力学相结合,探索血管损伤与疾病的关系及其病理机制,将是传统法医学的一项技术创新。本文综述了人体血管有限元模型的建立与发展,以及血管生物力学的研究进展。最后展望了有限元建模在法医病理学中的应用前景。
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引用次数: 0
[Forensic identification of lung contusion and laceration complicated with multiple pseudocysts: A case report]. [肺挫伤撕裂伤合并多发假性囊肿的法医鉴定1例]。
Pub Date : 2023-10-25 DOI: 10.12116/j.issn.1004-5619.2021.211006
明 安永, 志 威 张, 国 鹏 关
孟某,女,19岁,某年8月4日因“交通事故致左肩部、胸部疼痛,活动受限2 h”就诊。10月4日对孟某的损伤程度进行鉴定。.
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引用次数: 0
[Jinci declaration of Chinese forensic medicine]. 【中国法医学晋祠宣言】。
Pub Date : 2023-10-25 DOI: 10.12116/j.issn.1004-5619.2023.431002
会 中国法医学, 会 教育部高等学校法医学类专业教学指导委员
2023年10月16日,全国法医学领域的高校、科研机构以及最高人民法院、最高人民检察院、教育部、公安部、司法部和国家卫生健康委员会等部门的四百余位专家齐聚山西晋祠,共同参加“中国法医学科学技术发展论坛”。论坛期间,专家们回顾总结四十年来法医学教育、科研及社会服务成果,擘画新时代法医学事业发展未来,提出法医学新概念、新内涵和新定位,达成共识,由中国法医学会,教育部高等学校法医学类专业教学指导委员会联合发布“中国法医学 晋祠宣言”。.
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引用次数: 0
Application of SNaPshot Technology in Semen-Specific cSNP Genetic Marker. SNaPshot技术在精液特异性cSNP遗传标记中的应用。
Pub Date : 2023-10-25 DOI: 10.12116/j.issn.1004-5619.2021.510804
Rui-Yang Tao, Shou-Yu Wang, Chun-Yan Yuan, Ruo-Cheng Xia, Cheng-Tao Li

Objectives: To explore the feasibility of genetic marker detection of semen-specific coding region single nucleotide polymorphism (cSNP) based on SNaPshot technology in semen stains and mixed body fluid identification.

Methods: Genomic DNA (gDNA) and total RNA were extracted from 16 semen stains and 11 mixtures composed of semen and venous blood, and the total RNA was reverse transcribed into complementary DNA (cDNA). The cSNP genetic markers were screened on the validated semen-specific mRNA coding genes. The cSNP multiplex detection system based on SNaPshot technology was established, and samples were genotyped by capillary electrophoresis (CE).

Results: A multiplex detection system containing 5 semen-specific cSNPs was successfully established. In 16 semen samples, except the cSNP located in the TGM4 gene showed allele loss in cDNA detection results, the gDNA and cDNA typing results of other cSNPs were highly consistent. When detecting semen-venous blood mixtures, the results of cSNP typing detected were consistent with the genotype of semen donor and were not interfered by the genotype of venous blood donor.

Conclusions: The method of semen-specific cSNPs detection by SNaPshot technology method can be applied to the genotyping of semen (stains) and provide information for determining the origin of semen in mixed body fluids (stains).

目的:探讨基于SNaPshot技术在精液染色和混合体液鉴定中进行精液特异性编码区单核苷酸多态性(cSNP)遗传标记检测的可行性。方法:从16份精液染色液和11份精液与静脉血混合液中提取基因组DNA (gDNA)和总RNA,并将总RNA逆转录为互补DNA (cDNA)。在验证的精液特异性mRNA编码基因上筛选cSNP遗传标记。建立了基于SNaPshot技术的cSNP多重检测系统,并用毛细管电泳(CE)对样品进行基因分型。结果:成功建立了包含5个精液特异性csnp的多重检测系统。在16份精液样本中,除位于TGM4基因的cSNP在cDNA检测结果中出现等位基因缺失外,其他cSNP的gDNA与cDNA分型结果高度一致。在检测精静脉血混合物时,检测到的cSNP分型结果与供精者基因型一致,不受供精者基因型的干扰。结论:基于SNaPshot技术的精液特异性csnp检测方法可应用于精液(染色)的基因分型,为混合体液(染色)中精液来源的确定提供信息。
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引用次数: 0
期刊
Journal of Forensic Medicine
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