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Introduction: Analysis of a single tooth and nail can provide valuable forensic information, including year of birth, year of death, age, sex, DNA-profile, geographic residence during childhood and at time of death and drug exposure. The aim is to minimize the amount of used bodily material and to validate the applicability of a multidisciplinary sampling protocol.
Methods: A nail of the big toe, a tooth and blood of seven deceased individuals were collected postmortem. Collected materials were sampled and segmented in accordance with the multidisciplinary sampling protocol. DNA analysis was conducted on the pulp of the tooth, isotope analysis (Sr, Pb, O and C) on the enamel and C-, toxicological and tooth cementum annulation analysis on root segments. DNA-, isotope (Sr, Pb, O and C) -, toxicological-, and C -analysis were conducted on toenail segments. The acquired DNA profiles were compared with profiles acquired from blood.
Results: Material from seven deceased persons was analysed. 45 out of 56 analyses on dental samples were successful, constituting a success rate of 80%. Additionally, 27 out of 35 analyses were successful on nail samples, yielding a success rate of 77%. DNA-, toxicological and C- analyses performed better in nail than in tooth. Isotope analyses performed better in tooth than in nail. A profile with personal characteristics was constructed and matched for 62% of parameters with collected medical information.
Conclusion: The performed sampling protocol for simultaneous multidisciplinary forensic analysis on a single tooth and nail sample provided applicable results and valuable information.
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http://dx.doi.org/10.1007/s00414-024-03357-2 | DOI Listing |
BMJ Case Rep
August 2025
Department of Anesthesiology, National Hospital Organization Higashi Hiroshima Medical Center, Higashihiroshima, Hiroshima Prefecture, Japan.
Charcot-Marie-Tooth (CMT) disease is a progressive hereditary neuropathy that complicates anaesthesia because of neuromuscular-blocker sensitivity. Remimazolam, an ultra-short-acting benzodiazepine, has not yet been reported in CMT. We anaesthetised a woman in her 70s with CMT type 1A and cardiac sarcoidosis for femoral nail fixation under total intravenous anaesthesia with remimazolam and remifentanil.
View Article and Find Full Text PDFDespite numerous studies of droplet impact onto substrates, the splashing dynamics of droplets on biological material surfaces and its implications for infection transmission have rarely been studied. It is hypothesized that the splashing mechanism is influenced by the droplet size, the impact velocity, and the substrate wettability and morphology. The transmission of contamination from initial droplets or liquid films to biofilms upon impact is experimentally investigated.
View Article and Find Full Text PDFIndian J Dent Res
August 2025
Department of Pediatric and Preventive Dentistry, Manav Rachna Dental College, MRIIRS, SDS, Faridabad, Haryana, India.
Rationale: Ectodermal dysplasia is a genetic condition characterised by atypical development of organs derived from the embryonic ectoderm, such as teeth, nails, hair and sweat glands.
Clinical Signs: The most prevalent oral manifestation is hypodontia, which involves the absence of some or all primary and permanent teeth. Consequently, individuals with this condition often require dental prosthetic interventions during their formative years.
BMC Pregnancy Childbirth
August 2025
Department of Medical Genetics, NHC Key Laboratory of Healthy Birth and Birth Defect Prevention in Western China, The First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, China.
Background: Hypohidrotic ectodermal dysplasia (HED) is a rare genetic disorder that affects the development of the skin, hair, nails, teeth, and sweat glands. Due to its rarity, there are currently few methods that can be applied to facilitate its diagnosis during the prenatal period. Although a prenatal ultrasonographic examination will detect early signs of the disease, there are few reports on specific prenatal ultrasonographic features of ectodermal dysplasia.
View Article and Find Full Text PDFClin Genet
July 2025
Departments of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Türkiye.
Hypohidrotic ectodermal dysplasias are a genetic condition affecting ectoderm-derived structures such as hair, teeth, nails, and sweat glands, resulting from variations in the EDA, EDAR, EDARADD, and WNT10A genes. This study examined 32 cases from 25 unrelated families from Türkiye, identifying seven novel variants in the EDA, EDAR, and WNT10A genes. The distribution of genetic alterations across the cohort revealed that 44% of the families (11/25) harbored variants in EDA, whereas EDAR and WNT10A variants were identified in 32% (8/25) and 24% (6/25) of families, respectively.
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