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This systematic review deals with the last 10 years of research in analytical methodologies for the analysis of fingerprints, regarding their chemical and biological constituents. A total of 123 manuscripts, which fit the search criteria defined using the descriptor “latent fingermarks analysis,” were selected. Its main instrumental areas (mass spectrometry, spectroscopy, and innovative methods) were analyzed and summarized in a specific table, highlighting its main analytical parameters. The results show that most studies in this field use mass spectrometry to identify the constituents of fingerprints, both to determine the chemical profile and for aging. There is also a marked use of mass spectrometry coupled with chromatographic methods, and it provides accurate results for a fatty acid profile. Additional significant results are achieved by spectroscopic methods, mainly Raman and infrared. It is noteworthy that spectroscopic methods using microscopy assist in the accuracy of the analyzed region of the fingerprint, contributing to more robust results. There was also a significant increase in studies using methods focused on finding new developers or identifying components present in fingerprints by rapid tests. This systematic review of analytical techniques applied to the detection of fingerprints explores different approaches to contribute to future studies in forensic identification, verifying new demands in the forensic sciences and assisting in the selection of studies for the progress of research.

A total of 76 unrelated male patients with mild (n = 55) or moderate (n = 21) haemophilia A living in the southern Brazilian state of Rio Grande do Sul were studied by direct sequencing of all F8 26 exons, the 5' UTR and 3' UTR, intron-exon junctions and the promoter region. When no mutation was found, a multiplex ligation-dependent probe amplification analysis was performed. We identified the disease-causing mutations in 69 patients, who showed 33 different mutations: 27 missense, one small deletion, two small duplications and three splice site mutations. Seven missense and two splice site mutations were not previously reported in HAMSTeRS and were not identified in any current literature search. Nine recurrent mutations were found, one of them never described before (p.Tyr1786Phe). Haplotype analysis indicated that this mutation had originated in the Brazilian population as a single event in a common ancestor. The possible influence of these mutations in the determination of the disease was carefully considered, including bioinformatic tools. These data add to the general knowledge of the disease and can also be useful for HA diagnosis and detection of carriers in the southern Brazilian population.

Cannabis sativa L. is a substance widely used around the world for recreational and medicinal purposes. Oral fluid has been investigated as an alternative biological matrix for demonstrating the illegal use of cannabis, particularly in situations where