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While the shared DNA of identical twins dictates many of their similar physical traits, the development of fingerprints is a fascinating exception rooted in a combination of genetics and environment. The general patterns of arches, loops, and whorls are indeed inherited, which is why twins' prints may look very similar at a casual glance. However, the precise arrangement of the ridges and the fine details, known as minutiae, are not hardcoded in their genes. These unique characteristics are the result of a complex and chaotic series of events that occur during a specific window of fetal development.
Between the 10th and 24th week of gestation, the skin on the fingertips begins to form ridges. This process is influenced by a multitude of random factors within the womb's environment. The exact position of the fetus, the pressure and density of the amniotic fluid it touches, the length of the umbilical cord, and even subtle differences in blood pressure and finger growth rate all contribute to how the fingerprint ridges are laid down. This unique developmental journey ensures that every individual's fingerprints are distinct. Consequently, no two people have ever been found to have the same fingerprints, a principle that has become a cornerstone of forensic science.