Infertility & Genetics Package

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Understanding the Genetic Factors in Infertility

Infertility and recurrent pregnancy loss can be emotionally and physically challenging. While hormonal, anatomical, and environmental factors are often considered, genetics can play a significant role in reproductive outcomes.

Our London-based fertility genetics service provides comprehensive genomic assessment to help identify inherited factors that may contribute to infertility, recurrent miscarriage, or unsuccessful IVF cycles.

Understanding the Genetic Factors in Infertility

Infertility and recurrent pregnancy loss can be emotionally and physically challenging. While hormonal, anatomical, and environmental causes are often investigated, genetic factors may play a significant role in reproductive outcomes.

Why Genetics Matters

Certain inherited or chromosomal variations may affect embryo development, implantation, or pregnancy progression. Identifying these factors can provide clarity after unexplained infertility or repeated miscarriage.

Beyond Standard Fertility Tests

Standard fertility investigations may not detect subtle genetic contributors. Genomic assessment can uncover carrier status, chromosomal rearrangements, or inherited conditions influencing reproductive success.

Comprehensive Genomic Assessment in London

Our London-based fertility genetics service provides structured consultation and tailored genomic testing to identify inherited factors contributing to infertility, recurrent miscarriage, or unsuccessful IVF cycles.

Clarity through science. Understanding the genetic contribution to infertility enables informed reproductive planning and personalised guidance for future pregnancy decisions.

What Does the Assessment Include?

1. Comprehensive Reproductive History Review

A detailed consultation covering:

  • Previous pregnancies and outcomes

  • IVF or assisted conception history

  • Hormonal and fertility investigations

  • Family medical history

2. Carrier Screening

Expanded carrier screening can identify whether prospective parents carry genetic variants associated with inherited conditions that may affect offspring.

3. Chromosomal Analysis

Testing may include karyotyping or chromosomal microarray to detect balanced translocations or structural variations linked to miscarriage or implantation failure.

4. Advanced Genomic Testing

Where clinically indicated, options may include:

  • Expanded carrier panels

  • PGT (Preimplantation Genetic Testing) advisory input

  • Whole Exome or Whole Genome Sequencing

Testing strategies are carefully tailored to each couple’s clinical scenario.

How Genetic Testing Supports IVF and Family Planning

Genetic insight may:

  • Clarify reasons for repeated implantation failure

  • Identify inherited chromosomal rearrangements

  • Inform embryo selection strategies

  • Reduce the risk of transmitting serious genetic conditions

  • Guide decisions regarding donor gametes

  • Provide reassurance when results are normal

Results are interpreted in the context of reproductive planning and future pregnancy risk.

Post-Test Consultation and Ongoing Guidance

Results are typically available within four weeks. Your structured follow-up consultation is designed to provide clarity, reassurance, and a personalised reproductive plan based on your genomic findings.

💡 Hover over each box for more detailed information!
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Clear Explanation of Findings
Your results are explained in straightforward, clinically meaningful terms.
We carefully review identified variants, clarify their relevance to fertility or miscarriage risk, and address any uncertainties to ensure you fully understand the implications.
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Personalised Pregnancy Risk Assessment
Individualised evaluation of reproductive and future pregnancy risk.
We assess recurrence risk, carrier implications, and potential impact on embryo development to support informed decision-making.
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Guidance on IVF, PGT & Donor Options
Evidence-based recommendations tailored to your clinical scenario.
We discuss IVF strategies, Preimplantation Genetic Testing (PGT), donor options where relevant, and practical next steps aligned with your reproductive goals.
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Ongoing Specialist Support
Continued guidance and referral where necessary.
Where appropriate, we provide advice regarding natural conception strategies and coordinate referral to fertility specialists or multidisciplinary teams for further care.

Clarity, sensitivity, and evidence-based guidance. Our London fertility genetics service ensures you leave your consultation with a clear plan and confidence in your next steps.

Our London-Based Private Fertility Genetics Service

We offer a discreet, consultant-led reproductive genomics service in London. All testing is performed through accredited laboratories that meet UK regulatory standards.

We work collaboratively with fertility specialists, gynaecologists, and IVF clinics across the UK to ensure integrated and coordinated care.

Choosing Fertility Genetics Testing

Selecting the right fertility genetics service is a crucial step towards understanding reproductive risks, personalised guidance, and peace of mind. Several factors ensure the best possible experience for couples planning pregnancy or undergoing IVF.

Key Considerations: Expertise, Confidentiality, Personalised Care

Expertise: Choose a service led by experienced clinical geneticists specialising in reproductive genomics, recurrent miscarriage, and IVF challenges.

Confidentiality: Genetic information is deeply personal. Ensure the provider follows UK data protection regulations and maintains the highest level of privacy.

Personalised Care: Look for centres offering comprehensive consultations, tailored genomic testing, structured result interpretation, and ongoing support for couples and families.

Why Choose London Fertility Genetics?

Our Infertility & Genetics Package offers a private, consultant-led service with a patient-focused approach. From detailed pre-test consultation to structured post-test review, every step is designed to provide clarity and actionable guidance for your reproductive journey.

We collaborate with fertility specialists, IVF clinics, and gynaecologists across the UK to ensure integrated care. All genomic testing is conducted in accredited laboratories, fully compliant with UK medical standards.

Ready to take the next step? Book your consultation with our London fertility genetics experts today and gain personalised insight into reproductive risks and options.

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Frequently asked questions

In this section you can check frequently asked questions.

How common are genetic causes of infertility?

Genetic factors are identified in a proportion of couples with unexplained infertility or recurrent pregnancy loss. Chromosomal rearrangements and carrier status can significantly influence outcomes.

In many cases, yes. A combined assessment provides a clearer understanding of reproductive risk and ensures appropriate counselling.

Expanded carrier screening evaluates whether prospective parents carry genetic variants associated with inherited conditions, even if there is no family history.

Genetic testing does not guarantee success but can identify factors affecting implantation or miscarriage risk and inform embryo selection strategies where appropriate.

Yes. All consultations and genomic results are handled with strict confidentiality in accordance with UK data protection legislation.

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Dr. Ehsan Karimiani
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At London Genetics, booking your consultation couldn’t be simpler. Dr Ehsan Karimiani will take the time to listen, understand your background, and guide you through the right genetic testing or counselling options for you.

Whether you’re curious about how your DNA affects your health, medication response, or family risks, we’ll help you make informed choices with clarity and care.

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