Klinefelter syndrome: a comprehensive review beyond the 47 XXY karyotype

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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Autores principales:	Guevara Márquez, Diana Katerine, Méndez García, Germán Augusto
Formato:	info:eu-repo/semantics/article
Lenguaje:	spa
Publicado:	UNIVERSIDAD ANTONIO NARIÑO 2023
Materias:	Síndrome de Klinefelter (KS) aberración cromosómica Cariotipo 47XXY revisión sistemática chromosomal aberration Karyotype 47XXY systematic review. Klinefelter syndrome (KS)
Acceso en línea:	https://revistas.uan.edu.co/index.php/saywa/article/view/1588 https://repositorio.uan.edu.co/handle/123456789/11143
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