11. Define and interpret karyotypes (genetic anomalies to know: Down's, Turner's and Klinefelter's)
Solución de inteligencia artificial de Upstudy
Responder
Solución

¡Inicia sesión para desbloquear respuestas gratis!
Una plataforma de aprendizaje en la que confían millones de estudiantes y profesores reales.

Respondido por UpStudy AI y revisado por un tutor profesional
Mind Expander
Karyotyping is like flipping through the pages of a genetic book! It's a visual representation of an individual's chromosomes, typically arranged in pairs according to size and shape under a microscope. A karyotype can reveal genetic anomalies: for instance, Down syndrome often results from an extra copy of chromosome 21 (trisomy 21), while Turner syndrome is characterized by a missing or incomplete X chromosome (45, X0), typically seen in females. Klinefelter syndrome occurs when males have an extra X chromosome (47, XXY), leading to a variety of physical and reproductive characteristics. In the real world, karyotypes play a crucial role in prenatal screening and fertility treatments. They can help identify genetic disorders early, allowing parents to make informed decisions during pregnancy. Many couples facing infertility seek karyotyping to understand any underlying genetic issues that may be affecting their chances of conception. So, whether you're expecting or exploring, karyotyping provides valuable insights into your genetic health!
