Sperm Aneuploidy Screening/Testing in HSR Layout, Bangalore
Sperm Aneuploidy Screening (SAS) is a genetic test that analyzes the chromosomes in sperm to determine if they are carrying the correct number of chromosomes. SAS is used to detect chromosomal abnormalities in sperm, which can cause infertility and increase the risk of genetic disorders in offspring.
How Does SAS Work?
SAS involves analyzing a small sample of sperm for chromosomal abnormalities using a technique known as fluorescence in situ hybridization (FISH). FISH uses fluorescent probes to identify specific chromosomes and determine if they are present in the correct number.
What are the Benefits of SAS?
SAS can provide important information about the genetic health of sperm and can help identify if chromosomal abnormalities are present, which can cause infertility or increase the risk of genetic disorders in offspring. This information can be used to make informed decisions about treatment and can provide peace of mind for couples who are looking to start a family.
Who Should Consider SAS?
If you or your partner are experiencing infertility, or if there is a family history of genetic disorders, SAS may be right for you. Consult with your fertility specialist to determine if this test can help diagnose and treat your condition.
FAQ's on Sperm Aneuploidy Screening Treatment
Sperm aneuploidy screening may be recommended for couples who are planning to have children and have a history of infertility, repeated failed IVF cycles, or a family history of chromosomal disorders. It may also be recommended for couples who are older or have a higher risk of having a baby with a chromosomal disorder due to advanced maternal age.
Sperm aneuploidy screening is typically performed by analyzing a sample of sperm for the presence of abnormal chromosomes. This can be done through a variety of methods, including fluorescence in situ hybridization (FISH), comparative genomic hybridization (CGH), and next-generation sequencing (NGS).
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