Kleinfelter’s syndrome linking awareness with genetic insights Authors Komal Khan 2nd Year MBBS Student, Ziauddin University, Karachi, Pakistan https://orcid.org/0009-0006-4911-5118 Meenab Fatima 2nd Year MBBS Student, Ziauddin University, Karachi, Pakistan https://orcid.org/0009-0000-5667-6382 Syed Sameer Naqvi 2nd Year MBBS Student, Ziauddin University, Karachi, Pakistan https://orcid.org/0009-0000-8407-0740 DOI: https://doi.org/10.47391/JPMA.20631 Keywords: Klienfelter's Syndrome, Awarness, genetics, theraphy, comorbidities Abstract Madam, Klinefelter Syndrome is a genetic condition affecting males resulting in an additional X chromosome leading to multiple variations, including 47, XXY, 48, XXXY and 49, XXXXY (1). It is linked to chromosome non-disjunction that can happen during anaphase’s meiosis I, II or mitosis, leading to the presence of an extra X chromosome (1). Depending on genetic penetrance, Klinefelter’s syndrome leads to a wide range of phenotypes, the hallmarks being gynecomastia, hypergonadotropic hypogonadotropism and azoospermia (2). There are 250,000 men born with Klinefelter syndrome in the United States out of a male population of 148 million, and the condition affects 3% to 4% of male births (3). Nevertheless, despite increased awareness and concern for people born with it, research on this hereditary condition in Pakistan remains limited. Increasing public awareness of KS beyond medical circles is crucial to ensure individuals receive the resources they need. This condition presents as a male with effeminate features such as gynecomastia and underdeveloped genitalia (2). Additionally, the patient may suffer from infertility, cardiovascular symptoms, cerebrovascular symptoms, metabolic syndrome and an increased risk of other comorbidities (4). Cardiovascular mortality is higher in those with Klinefelter’s Syndrome due to aortic valve anomalies, pulmonary embolism, peripheral vascular disease, and deep vein thrombosis. (4) Fortunately, a lot has changed in terms of therapy possibilities. Some males with KS can father children by testicular sperm extraction (TESE). (5) According to studies, collecting sperm using TESE has a 40% success rate, and employing an intracytoplasmic sperm injection (ICSI) technique results in a 43% pregnancy rate per cycle. (5) Many of the symptoms and effects of Klinefelter syndrome can be managed, and in some cases, even prevented with proper treatment, such as hormone therapy period. (4) With the right care, people with Klinefelter's syndrome can safely become parents and lessen the impact the condition has on their day-to-day activities (4,5). Downloads Full Text Article Published 2025-03-18 How to Cite Khan, K., Fatima, M., & Naqvi, S. S. (2025). Kleinfelter’s syndrome linking awareness with genetic insights. Journal of the Pakistan Medical Association, 75(04), 690–690. https://doi.org/10.47391/JPMA.20631 More Citation Formats ACM ACS APA ABNT Chicago Harvard IEEE MLA Turabian Vancouver Download Citation Endnote/Zotero/Mendeley (RIS) BibTeX Issue Vol. 75 No. 04 (2025): APRIL Section STUDENT'S CORNER LETTER TO THE EDITOR License Copyright (c) 2025 Journal of the Pakistan Medical Association This work is licensed under a Creative Commons Attribution 4.0 International License.