Reading Time: 2 minutesIntroduction to Klinefelter Syndrome Klinefelter syndrome, a genetic condition affecting approximately 1 in 500 to 1,000 newborn males in the United States, is characterized by an additional X chromosome, resulting in a karyotype of XXY. This condition can lead to a variety of physical, developmental, and cognitive challenges. Among the most common symptoms are reduced testosterone levels, infertility, and delayed or incomplete puberty. The management of Klinefelter syndrome often involves a multidisciplinary approach, with hormone replacement therapy playing a pivotal role. Understanding Humatrope Humatrope, a recombinant human growth hormone (somatropin), has emerged as a significant therapeutic agent in the management … Continue reading →