Klinefelter Syndrome(47 XXY Syndrome; KS)
by
Cynthia M. Johnson, MA DefinitionKlinefelter syndrome (KS) happens in men who have more than one X chromosome (XXY).
CausesMales have a single X chromosome from their mother and a single Y one from their father. Males with KS get at least one extra X from either parent. Risk FactorsThere are no known risk factors for KS. SymptomsSymptoms may not be found until puberty or later. Children may have problems with:
Teens may have:
Adults may have:
DiagnosisThe doctor will ask about your symptoms and health history. A physical exam will be done. KS is diagnosed with a genetic test. Blood tests may also be done. TreatmentThere is no cure. The goal is to manage symptoms. Choices are:
PreventionThere are no known guidelines to prevent KS. RESOURCES:The Association for X and Y Chromosome Variations http://www.genetic.org National Institute of Child Health and Human Development http://www.nichd.nih.gov CANADIAN RESOURCES:Canadian Psychiatric Association http://www.cpa-apc.org Canadian Psychological Association http://www.cpa.ca References:Groth KA, Skakkebæk A, et al. Clinical review: Klinefelter syndrome--a clinical update. J Clin Endocrinol Metab. 2013 Jan;98(1):20-30.
Klinefelter syndrome. EBSCO DynaMed website. Available at:
https://www.dynamed.com/condition/klinefelter-syndrome. Accessed November 5, 2020.
Klinefelter syndrome (KS): Overview. National Institute of Child Health and Human Development website. Available at: ...(Click grey area to select URL) Accessed November 5, 2020. Last reviewed September 2020 by EBSCO Medical Review Board
Kari Kassir, MD Last Updated: 5/11/2021 |
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