Certified Medical Magazine by WMA, ACSA, HON
FAQs
0
Menu

Is Klinefelter syndrome a genetic disease?

By José Luis de Pablo.
Last Update: 09/21/2018

Klinefelter syndrome or 47,XXY is a genetic abnormality that occurs as a consequence of an incorrect division of homologous chromosomes during meiosis, which give raise to the gametes of one of the parents. It can also occur during the first divisions of the zygote.

Males affected by it suffer from hypogonadotropic hypogonadism, gynecomastia, learning disabilities, and infertility. It is the most common genetic disease in males. Some men, however, do not have symptoms, and they don't know that they have this condition until they are adults and have infertility issues.

Suggested for you: Klinefelter Syndrome (XXY Syndrome) – Symptoms, Causes & Fertility.

 José Luis de Pablo
José Luis de Pablo
BSc, MSc, PhD
Senior Clinical Embryologist
Double Degree in Biology and Biochemistry from the University of Navarra. Master’s Degree about the Theoretical Basis and Laboratory Procedures in Assisted Reproduction from the University of Valencia (UV). Senior Clinical Embryologist from the ESHRE and ASEBIR Certification in Clinical Embryology. More than 15 years of experience as the director of IVF labs.
Senior Clinical Embryologist. Double Degree in Biology and Biochemistry from the University of Navarra. Master’s Degree about the Theoretical Basis and Laboratory Procedures in Assisted Reproduction from the University of Valencia (UV). Senior Clinical Embryologist from the ESHRE and ASEBIR Certification in Clinical Embryology. More than 15 years of experience as the director of IVF labs.
We use own cookies and third party cookies to offer you personalized ads and gather statistical data. If you continue the navigation we understand that you accept our cookies policy.