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:

Tipo de recurso:

Article of journal

Fecha de publicación:

2023

Institución:

Universidad Antonio Nariño

Repositorio:

Repositorio UAN

Idioma:

spa

OAI Identifier:

oai:repositorio.uan.edu.co:123456789/11143

Acceso en línea:

https://revistas.uan.edu.co/index.php/saywa/article/view/1588
https://repositorio.uan.edu.co/handle/123456789/11143

Palabra clave:

Síndrome de Klinefelter (KS)
aberración cromosómica
Cariotipo 47XXY
revisión sistemática
chromosomal aberration
Karyotype 47XXY
systematic review.
Klinefelter syndrome (KS)
Klinefelter syndrome (KS)

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Derechos de autor 2022 Diana Katerine Guevara Márquez, Germán Augusto Méndez García