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© 2020 S. Karger AG, Basel.BACKGROUND Two loci (CHD7 and SOX1 underlying Kallmann syndrome (KS) were discovered through clinical and hereditary analysis of CHARGE and Waardenburg syndromes, conditions that include congenital anosmia brought on by olfactory bulb flaws (CA/OBs) and congenital hypogonadotropic hypogonadism (CHH). We hypothesized that other applicant genetics for KS could possibly be found by analyzing unusual syndromes showi