Síndrome de Klinefelter: una revisión integral más allá del cariotipo 47 XXY

Klinefelter syndrome is a pathological condition caused by a chromosomal aberration in males, resulting in the most common alteration of sex chromosomes in humans, characterized by a karyotype of 47 XXY. Its prevalence ranges from 85 to 250 cases per 100,000 live births annually. The absence of clin...

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Bibliographic Details

Main Authors:	Guevara Márquez, Diana Katerine, Méndez García, Germán Augusto
Format:	Digital
Language:	spa
Published:	UNIVERSIDAD ANTONIO NARIÑO 2023
Subjects:	Síndrome de Klinefelter (KS) aberración cromosómica Cariotipo 47XXY revisión sistemática chromosomal aberration Karyotype 47XXY systematic review. Klinefelter syndrome (KS)
Online Access:	https://revistas.uan.edu.co/index.php/saywa/article/view/1588
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