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First of all, Preimplantation genetic screening is a vital pre-conception diagnostic service that identifies hidden DNA risks affecting male and female reproductive success. Essentially, combining Next-Generation Sequencing (NGS) expanded carrier panels, G-banded karyotyping, and Y-chromosome microdeletion assays (AZFa, AZFb, AZFc), Preimplantation genetic screening detects single-gene carrier states (Thalassemia, SMA, CF) and structural chromosomal translocations with 99.9% clinical accuracy. Consequently, prospective parents obtain critical guidance for natural conception or IVF with PGT.
Furthermore, book your Preimplantation genetic screening at Henotic Diagnostics for authoritative diagnostic accuracy. In addition, our accredited laboratory operates 24/7 with expert genetic counseling and home sample collection facilities.
To begin with, Preimplantation genetic screening is a proactive clinical evaluation designed to identify asymptomatic genetic or chromosomal factors that impair fertility or threaten future pregnancies. At the same time, experts at Henotic Diagnostics deploy advanced Next-Generation Sequencing (NGS) panels to screen prospective couples before pregnancy or IVF treatment.
Furthermore, comfortable reception lounge providing supportive registration for couples undergoing fertility screening draws
What Does Fertility Genetic Screening Evaluate?
Specifically, Preimplantation genetic screening evaluates silent autosomal recessive carrier mutations (such as Beta Thalassemia, SMA, and Cystic Fibrosis), Y-chromosome microdeletions in males with low sperm count, Fragile X premutations in females with low ovarian reserve, and balanced chromosomal translocations. Consequently, identified carrier couples prevent inherited genetic disorders in offspring through pre-conception planning or PGT-M embryo selection. As a result, parents achieve reproductive confidence. In fact, to review genetic screening facts, consult the NIH NHGRI Genetic Testing Fact Sheet.
Furthermore, combining G-banded karyotyping, and Y-chromosome microdeletion assays (AZFa, AZFb, AZFc) for structural chromosomal translocations detection
What is Fertility Genetic Screening?
In general, genetic carriers carry one normal gene copy and one mutated gene copy without showing medical symptoms. Essentially, Preimplantation genetic screening extracts constitutional DNA from blood leukocytes and sequences high-risk disease genes using high-depth NGS platforms and cytogenetic karyotyping. Therefore, joint couple risks are definitively mapped before pregnancy. Additionally, to read about clinical reproductive genetics, examine the Nature Reviews Genetics journal.
Additionally, high-throughput NGS sequencers analyze DNA sequences to detect carrier mutations and microdeletions
What Does Fertility Genetic Screening Check?
Overall, Preimplantation genetic screening evaluates key reproductive health pillars:
Key Screening Panels Evaluated
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Autosomal Recessive Carrier Panel: First, screens 100+ genes including HBB (Thalassemia), SMN1 (SMA), and CFTR (Cystic Fibrosis).
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Male Spermatogenic Factor (AZF Panel): Second, screens Y-chromosome AZFa, AZFb, and AZFc microdeletions in men with severe oligospermia or azoospermia.
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Female Ovarian Reserve & Fragile X: In addition, quantifies FMR1 CGG repeat expansions associated with premature ovarian failure. Review the ClinVar NCBI variant database.
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Parental Karyotype Translocation Check: Finally, screens G-banded chromosomes for balanced Robertsonian or reciprocal translocations.
In addition, bioinformatic software maps carrier variants against global ACMG pathogenicity databases
When Is Fertility Genetic Screening Recommended?
For example, reproductive specialists recommend Preimplantation genetic screening for all couples planning pregnancy or preparing for IVF treatment. In particular, screening is essential for couples with consanguineous marriages, unexplained infertility, or a history of recurrent pregnancy loss. Moreover, couples undergoing ICSI utilize fertility screening to verify Y-chromosome deletion risks. In addition, to review ASRM guidelines, examine the ASRM Reproductive Medicine Guidelines.
Moreover, expert clinical geneticists provide pre-conception genetic counseling to interpret screening findings for couples
Clinical Value: Pre-Conception Genetic Screening vs. Late Post-Natal Diagnosis
Ideally, couples should complete Preimplantation genetic screening before attempting conception because pre-conception discovery unlocks maximum reproductive choices, including IVF with PGT-M or donor gametes. In contrast, post-natal diagnosis occurs only after an affected child is born. Indeed, to review global reproductive health standards, consult the WHO Infertility & Global Reproductive Health Fact Sheet.
Fertility Genetic Screening Cost Guide
Fertility Genetic Screening Panel
Approximate Cost (₹)
Single Partner Core Carrier & Karyotype Screen
First, single partner core screening is ₹9,500 – ₹14,000.
Male Infertility Screen (Karyotype + Y-AZF Microdeletion)
Second, male infertility screening costs ₹12,000 – ₹16,000.
Female Infertility Screen (Karyotype + Fragile X FMR1)
In addition, female infertility screening costs ₹12,000 – ₹16,000.
Comparison: Sequential Partner Screening vs. Simultaneous Couple Screening
On one hand, Sequential Partner Screening evaluates one partner first and tests the second partner only if mutations are found, whereas Simultaneous Couple Screening evaluates both partners at once for rapid pre-conception timeline assurance. Consequently, clinicians recommend simultaneous screening when IVF cycles are scheduled. In fact, review the PubMed Clinical Fertility Genetic Screening Review.
Feature
Sequential Partner Screening
Simultaneous Couple Screening
Initial Cost
First, lower initial cost (One partner tested).
However, full couple panel cost upfront.
Turnaround Speed
Second, slower (Requires 2 sequential rounds).
In contrast, fastest total turnaround (7-10 days).
First, Fertility Genetic Screening is a preventive genomic evaluation that tests male and female DNA to identify hereditary gene mutations, carrier states, and chromosomal rearrangements before conception or IVF.
What disorders are detected in Fertility Genetic Screening?▼
In addition, the screening evaluates Beta Thalassemia, Spinal Muscular Atrophy (SMA), Y-chromosome AZF microdeletions, CFTR gene mutations, Fragile X premutations, and balanced Robertsonian translocations.
When should couples undergo Fertility Genetic Screening?▼
Generally, screening is recommended prior to conceiving naturally, before initiating IVF / ICSI treatments, or following unexplained miscarriages.
Do I need to fast before Fertility Genetic Screening?▼
Because genetic screening evaluates permanent germline cellular DNA, fasting is unnecessary.
How long until I receive diagnostic Fertility Genetic Screening results?▼
Fortunately, detailed clinical bioinformatic screening reports are delivered within 7 to 14 business days.
What is the cost of Fertility Genetic Screening?▼
Overall, high-precision Fertility Genetic Screening ranges from ₹9,500 to ₹28,000 depending on panel selection (Single Partner Karyotype, Male Microdeletion Panel, or Couple Expanded Carrier Screen).
Quick Appointment Booking
Schedule your Fertility Genetic Screening with accredited reproductive genetic experts.
MBBS, MD (Reproductive Genetics) · 15+ Years Clinical Experience
Furthermore, your Fertility Genetic Screening reports are evaluated by accredited reproductive endocrinologists and clinical geneticists. Consequently, comprehensive reports empower couples with clear pre-conception guidance.
Real feedback from couples who completed Fertility Genetic Screening with us.
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“Pre-conception Fertility Genetic Screening identified that both my husband and I carried Beta Thalassemia mutations. Furthermore, IVF with PGT-M led to a healthy baby boy!”
– Kavita N.
Verified Patient Review
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“Comprehensive couple screening report delivered in 10 days. In addition, post-test genetic counseling gave us complete peace of mind.”
– Suresh B.
Verified Patient Review
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“Premier NABL accredited laboratory for reproductive screening. Henotic Diagnostics is our trusted partner for pre-conception genetic workups.”
Common Questions About Fertility Genetic Screening
You can book your Fertility Genetic Screening appointment at our Navi Mumbai center through multiple convenient channels: call us directly at 088793 27184, send a WhatsApp message for instant booking, or use the online booking form on our website. Walk-in appointments are also welcome based on slot availability. We recommend advance booking to ensure zero wait times.
Yes, Henotic Diagnostics Navi Mumbai is empanelled with all major insurance companies and TPAs (Third Party Administrators) including Star Health, ICICI Lombard, New India Assurance, HDFC Ergo, Max Bupa, Bajaj Allianz, and many more. We offer cashless processing for Fertility Genetic Screening where applicable. Please carry your insurance card and a valid ID for seamless processing.
At Henotic Diagnostics Navi Mumbai, most Fertility Genetic Screening reports are delivered within 2-6 hours for routine tests. Critical and urgent reports are expedited on a priority basis. All reports are delivered digitally via WhatsApp, email, and our secure online patient portal. Hard copies are also available at the center upon request. You will receive an SMS/WhatsApp notification the moment your report is ready.
Henotic Diagnostics Navi Mumbai operates 24 hours a day, 7 days a week, including Sundays and public holidays. This means you can schedule your Fertility Genetic Screening at a time that is most convenient for you — early morning, late evening, or even overnight for emergency requirements. Our radiology and pathology departments maintain round-the-clock availability.
Yes, Henotic Diagnostics Navi Mumbai is fully accredited by NABL (National Accreditation Board for Testing and Calibration Laboratories) and ISO 9001:2015 certified. Our radiology equipment also complies with AERB (Atomic Energy Regulatory Board) safety standards. These accreditations ensure that every Fertility Genetic Screening performed at our facility meets the highest national and international quality benchmarks for accuracy, safety, and reliability.
