ORIGIN, TREATMENT AND PREVENTION OF KLINEFELTER SYNDROME

Authors

  • Sahibova Mavluda Jo’rayevna Andijan State Medical Institute , Uzbekistan

Keywords:

Klinefelter syndrome , treatment , drug , XXY, XY, chromosome.

Abstract

Klinefelter syndrome (KS), also known as 47,XXY, is an aneuploid genetic condition where a male has an additional copy of the X chromosome. The primary features are infertility and small, poorly functioning testicles. Usually, symptoms are subtle and subjects do not realize they are affected. Sometimes, symptoms are more evident and may include weaker muscles, greater height, poor motor coordination, less body hair, breast growth, and less interest in sex. Often, these symptoms are noticed only at puberty. Intelligence is usually average, but reading difficulties and problems with speech are more common.

References

Fogel F., Matulskiy A., Genetika cheloveka, v 3-x tomax, per. s angl., M., 1990.

Muxsin Zokirov.[1]

www.google.com

www.wikipedia.com

https://www.webmd.com/men/klinefelter-syndrome

Published

2023-09-22

How to Cite

Sahibova Mavluda Jo’rayevna. (2023). ORIGIN, TREATMENT AND PREVENTION OF KLINEFELTER SYNDROME. Ethiopian International Journal of Multidisciplinary Research, 10(09), 95–98. Retrieved from https://eijmr.org/index.php/eijmr/article/view/175