Karyotype
The Karyotype Test is a fundamental genetic analysis in the study of fertility. It allows for the detection of alterations in the number or structure of chromosomes that can cause infertility, recurrent miscarriages, congenital malformations or developmental delay. These anomalies are responsible for up to 50% of miscarriages in the first trimester.
Why get a Karyotype Test?
The Karyotype Test allows for the detection of genetic alterations that may be affecting your fertility or causing recurrent miscarriages. It is an essential test before starting assisted reproduction treatment, as it provides a clear diagnosis and helps to personalise the medical approach.
This study identifies chromosomal anomalies that often do not present symptoms but directly influence conception and embryonic development. Additionally, it allows for the prevention of the transmission of genetic alterations to offspring and enables safer and more effective medical decisions.
What are the benefits?
Accurate diagnosis
Grain greater diagnostic clarity before starting fertility treatments with medical guidance based strictly on your unique genetic profile.
Support
Receive personalised, compassionate support from our team of biotechnology experts throughout your journey.
Reproductive success
Maximise your chances suena muchísimo más natural en el sector de la fertilidad que achieve the highest probability
Who is it for?
- Couples with recurrent miscarriages or infertility.
- Couples who are about to start an assisted reproduction process.
- Individuals with suspected congenital malformations.
- Individuals with developmental delay.
Test procedure
Sample collection
Collection of peripheral blood in heparin tubes by our laboratory team. It is a quick, minimally invasive procedure.
Preparation
The procedure is quick and simple: no prior preparation or fasting is required.
Analysis
A thorough laboratory analysis is performed to detect possible alterations in the number or structure of chromosomes.
Results
A detailed interpretive report is sent directly to your doctor to coordinate the clinical approach.
The Karyotype Test identifies genetic alterations before they manifest clinically, facilitating early medical intervention. Its application in preventive medicine helps mitigate reproductive risks, plan safe pregnancies, and prevent the transmission of chromosomal abnormalities to offspring.