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4 cze 2024 · Klinefelter syndrome (KS) is a chromosome variation affecting around 1 in 660 males in which an extra X chromosome is present, resulting in a genetic karyotype of 47,XXY. Karyotype analysis is required for definitive diagnosis.
28 paź 2024 · For men with Klinefelter syndrome, here are some tips: Work with your doctor to manage your health and avoid issues such as osteoporosis. Discuss family planning options with your doctor.
12 lis 2023 · This activity reviews the evaluation and treatment of Klinefelter syndrome and the role of the interprofessional team in managing this condition. Objectives: Identify the cause of Klinefelter syndrome. Screen individuals at risk of Klinefelter syndrome, especially during early childhood and puberty.
29 paź 2024 · Klinefelter syndrome can be caused by: One extra copy of the X sex chromosome in each cell (XXY), the most common cause. An extra X sex chromosome in some of the cells. This is called mosaic Klinefelter syndrome and may result in fewer symptoms.
29 paź 2024 · Treatment for Klinefelter syndrome is based on symptoms and may include: Testosterone therapy. Starting at the time of the usual onset of puberty, testosterone therapy can be given to help stimulate changes that typically occur at puberty.
In 1959, these men with Klinefelter syndrome (KS) were discovered to have an extra X chromosome (genotype XXY) instead of the usual male sex complement (genotype XY).
15 lut 2013 · Early detection of this syndrome is recommended in order to offer treatment and intervention at the appropriate ages and stages of development for the purpose of preventing osteopenia/osteoporosis, metabolic syndrome, and other medical conditions related to hypogonadism and to the XXY as well as minimizing potential learning and psychosocial ...
