SEVİM BÜŞRA KORKMAZ,MUSTAFA GAHNUG,SAİME ERGEN DİBEKLİOĞLU,BERAY SELVER EKLİOĞLU,MEHMET EMRE ATABEK

  • MUSTAFA GAHNUG: NECMETTİN ERBAKAN ÜNİVERSİTESİ
  • BERAY SELVER EKLİOĞLU: NECMETTİN ERBAKAN ÜNİVERSİTESİ
  • MEHMET EMRE ATABEK: NECMETTİN ERBAKAN ÜNİVERSİTESİ
  •  Year : 2023
  •  Vol : 3
  •  Issue : 2
  •  Page : 94-96
ABSTRACT
Klinefelter Syndrome (KS), the most common sex chromosome abnormality in men, is also one of the leading causes of male infertility. Generally, these individuals with 47, XXY karyotype are diagnosed during adulthood, during infertility examinations. In the adolescence period, there may be an increase in height growth rate, euicoid body structure, delay or pause in puberty, gynecomastia, small volume and hardness of the testicles, and less facial and body hair. In this article, an adolescent case who presented with the complaint of rapid stature, was diagnosed with KS, and was diagnosed with KS in the chromosome analysis of 47, XXY, which was performed by suspecting KS with clinical and laboratory data, is presented.

Key words: Klinefelter syndrome, tall, 47, XXY
Cite this Article As : Korkmaz SB, Gahnug M, Ergen Dibeklioğlu S, Selver Eklioğlu B, Atabek ME. Boy Uzama Hızında Artışla Gelen Klinefelter Sendromlu Olgu Sunumu. Mev Med Sci. 2023;3(2):94-96

Conflict of interest : Yok

This article is published under the CC BY-NC 4.0 license.
Mevlana Tıp Bilimleri
2023, Vol3, Issue2
E-ISSN: 2757-976X
Received : , Accepted : , Published Online :