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What is Genetic Counselling?

Genetic Counselling is a specialised healthcare service that assists individuals, couples, and families in understanding how genetics can affect their health and well-being.

The goal of genetic counselling is to:

  • Assess risk of inherited conditions or genetic disorders.
  • Provide clear information about genetic findings, testing options, and medical implications.
  • Support informed decision-making regarding healthcare, family planning, and lifestyle choices.
  • Offer emotional support while navigating complex and sometimes sensitive genetic information.
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We are recognised as The Most Trusted Genetics Brand, “CYTOGeNeOM”, (Devoted to Genetic Disorders) established in 2017 by an AIIMS, New Delhi alumnus, on a mission to empower millions of couples, parents, children, and cancer warriors through our trusted genetic counselling services.

Our team of dedicated doctors, scientists, and experienced genetic counsellors combine medical expertise with compassionate guidance—sharing knowledge and insights to support informed decisions with clarity and confidence.

Our approach blends medical expertise, advanced laboratory support, and compassionate counselling to deliver the highest standards of care. We believe in open, approachable dialogue, where genetic findings are explained in the context of the latest technologies, scientific research, and diagnostic insights. Every consultation is led by seasoned genetic experts, making complex information clear, accessible, and actionable.

  • Expertise – PhD-level knowledge in the field of clinical genetics with 15+ years of professional experience.
  • Personalised Care – Every session is tailored to the patient’s medical and family background.
  • End-to-End Support – From test selection to interpretation and long-term planning.
  • Compliance & Quality – Services aligned with global best practices and ISO/NABL standards.

Our Genetic Counselling Approach:

  • Comprehensive Case Review – Medical history, family pedigree & risk assessment.
  • Education & Communication – Clear explanation of inheritance, recurrence risks & test options.
  • Decision Support – Facilitating informed reproductive and healthcare decisions.
  • Psychosocial Support – Addressing emotional, cultural, and ethical considerations.
  • Integration with Care Teams – Working alongside clinicians, IVF specialists, and laboratories.
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To be leader in genetics counselling services offered in the friendliest manner providing with aid from recent developments in genetic technologies and helping millions of patients to get the personalized care.

Our Core Services

Preconception & Prenatal Genetic Counselling

  • Carrier screening for common genetic disorders (e.g., Thalassemia, SMA, Cystic Fibrosis)
  • Risk assessment for advanced maternal/paternal age
  • Guidance on prenatal screening & diagnostic options (NIPT, CVS, Amniocentesis)
  • Support for couples with a history of recurrent pregnancy loss or congenital anomalies

Paediatric & Rare Disease Genetic Counselling

  • Evaluation of congenital malformations, developmental delay, or intellectual disability
  • Counselling for metabolic, neuromuscular, and rare genetic disorders
  • Family-based genetic testing & recurrence risk assessment
  • Support with multidisciplinary management and clinical trial referrals

Oncology Genetic Counselling

  • Risk evaluation for hereditary cancer syndromes (BRCA1/2, Lynch syndrome, etc.)
  • Guidance on genetic testing & interpretation of results
  • Personalised risk reduction and surveillance strategies
  • Cascade testing for family members at risk

Adult & Predictive Genetic Counselling

  • Neurogenetic disorders (Huntington’s, Charcot-Marie-Tooth, Ataxias)
  • Cardiogenetics (Hypertrophic cardiomyopathy, Long QT, Marfan syndrome)
  • Pharmacogenetic insights for precision medicine
  • Predictive and presymptomatic testing

Haematology & Immunogenetics Genetic Counselling

  • Genetic counselling for Thalassemia, Sickle cell anaemia, and haemoglobinopathies
  • Severe Combined Immunodeficiency (SCID) & Primary Immunodeficiency Disorders
  • Coordination for bone marrow transplant-related genetic evaluation

Assisted Reproduction & IVF-related Genetic Counselling

  • Preimplantation Genetic Testing (PGT) for aneuploidy or monogenic disorders
  • Genetic risk assessment for couples undergoing IVF/ICSI
  • Donor gamete considerations (legal/ethical aspects)
  • Reproductive options for carriers of genetic disorders

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Dr. Ashish Fauzdar

Founder, CYTOGeNeOM

Dr Ashish Fauzdar, an alumnus of AIIMS New Delhi, holds a doctorate in Reproductive Genetics from the All-India Institute of Medical Sciences. He brings over 23 years of experience in laboratory genetics and genomics across academic institutions, hospitals, reputed ART/infertility clinics, and diagnostic laboratories. He has authored 25+ peer-reviewed publications, contributed book chapters, and presented at national and international conferences.

Expertise: Extensive clinical genetics experience in karyotyping, FISH, chromosome microarray (CMA), and interpretation of clinical and whole exome sequencing data across multiple sequencing/NGS platforms.

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CYTOGeNeOM

Our professionals have made a promise to put your health first and to be there for you before, during and after the treatment. You can be sure that our specialists will guide you through the medical journey from start to finish!

  • Phone Number

    Phone Number

    +91-9821555406

  • Email

    Email Address

    info@cytogeneom.com

  • Address

    Address

    Pillar 17, D-82A, Maharaja Agrasen Marg, Noida, 201301,UP,IN

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