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In-vitro fertilization (IVF) has proven to be an invaluable solution for couples struggling to conceive naturally, offering renewed hope while managing uncertainties through infertility treatment and transference of an embryo from the lab. While genetic testing provides hope to prospective parents looking forward to becoming pregnant through IVF treatment, its efficacy should not be discounted; its presence should serve as an invaluable aid towards increasing chances of a successful outcome and ensure you make every opportunity count!<br><br>Visit: https://drmazenivf.com/genetic-testing-pregnancy/
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UNDERSTANDING GENETIC TESTING IN IVF WITH DR. MAZEN IVF
Genetic Testing’s Role in IVF Genetic testing offers couples seeking IVF treatments an efficient and precise means of tackling any obstacles related to conception that might arise during treatment, thus playing an essential part. Here is how it plays its part:
1. Aneuploidy Screening Aneuploidy refers to any deviations in chromosomal numbers that lead to fertility issues, miscarriages, or developmental disorders. More likely than ever to arise as we age – particularly women as they become less fertile as time progresses while their quality of eggs decreases. 2. Diagnosing Single- Gene Disorders Single-gene conditions like cystic fibrosis, sickle cell anemia, and Huntington’s disease arise as the result of mutations to specific genes; couples who share family histories that include such conditions run an increased risk of passing them onto their offspring.
3. Addressing Genetic Blood Disorders Thalassemia, a genetic blood condition with a 25 percent risk for transmission through couples carrying both carriers, presents couples who share that risk a unique challenge: one child of each carrier could inherit its condition at birth.
How Does Genetic Testing in IVF Work? 2. Genetic Analysis 1. Embryo Development
Advanced Genetic Testing Techniques Next-Generation Sequencing (NGS): This cutting-edge genetic sequencing technology sequences large amounts of DNA quickly, revealing genetic variations with unparalleled precision and speed. Comparative Genomic Hybridization (CGH): CGH compares embryo DNA against reference DNA samples to detect imbalances, such as duplications or deletions that might compromise development or trisomy (such as Down Syndrome).
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