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Comprehensive andPersonalized GeneticTesting for Obstetrics, Gynaecology and Feto-Maternal Units

Genomic Precision Diagnostic

GPDx

What are the benefits ofIntegrating Genomics intoMedical Decisions?

Diagnostic testingIndications

For most of the clinical conditions genetic testing is the only way to make an accurate diagnosis and help avoid additional unnecessary clinical investigations.

Reduces the uncertainty in a differential diagnosis and provides a directed focus for the specialist to provide appropriate treatment.

Decreases referrals from specialist to specialist, allowing a high quality patient care.

Can guide the specialist in choosing the most suitable downstream tests, therapy and support for the patient.

- Identify genetic conditions that could causedisease in newborn babies.- Prevent complications and increase life expectancy.

Neonatal Screening/Diagnostic

- Couples and families who want to know if they carrya genetic condition and determine if they are at riskof having a child with a genetic disease.

Preconception Prevention

- Family history of a genetic condition (hereditary disor-der,chromosomal alteration...).- High risk established using screening methods: first and second trimester, cffDNA (NIPT).- Ultrasound findings of a genetic condition: (genetic disorder, chromosomal alteration,...).- Pregnancy with poor evolution or miscarriage.

High Risk Pregnancies

Our experienced Geneticists guideyou throughout the whole diagnostic process

Dr. Lova SatyanarayanaPhD Human Genetics

Dr. Garcia‐PlanellsPhD Human Genetics

Dr. Julio MartínPhD Molecular Genetics

Diagnostic Technologies

Complete DNA test to identify mutations in over24,000 genes related to complex genetic problems.

WHOLE EXOME/GENOMESEQUENCING(WES/WGS)

Choose your panel andbenefit from the highestdiagnostic accuracy.

IGX PRECISIONPANELS

Many genetic diseasesare caused by changesor variants in a singlegene. We have acomprehensive range of tests to cover your needs.

Gold standard for thedetection of Copynumber variations (CNVs).

SINGLE GENEANALYSIS

CMA: CHROMOSOMALMICROARRAY TESTING

Get supported by our experienced and high skilled teamto choose the best Genetic testing

DIAGNOSTIC SERVICES for all life stages

PRECONCEPTION

To study the ecosystem of the endometrial bacteriaand recommend treatments options (antibiotic or probiotic).

To understand the couple's risk of having an affectedchild with a genetic disorder.

To confirm the genetic disorder of the affected baby and understand the risk of having another affected child.

ENDOMETRIO Analysis

Couple Screening before conceiving

Couple Diagnostic After having an affected baby

Prenatal Genetic Diagnosis is a service that identifies geneticalterations in the fetus that can lead to a disorder duringpregnancy or the neonatal period that is clinically actionable.

Testing can be done through non invasive or invasivetechniques.

To identify if the miscarriage was caused by a genetic disorder or chromosomal abnormalities.

Non InvasivePrenatal analysisusing Non-invasive prenatal test (NIPT)

Invasive Prenatalanalysisusing Invasive prenatal testCVS and Amniocentesis

Miscarriage analysisusing Product of conception

Prenatal

Neonatal

To screen or diagnose new babies for genetic conditions.

New-Born analysis To identify genetic disorders in new-born babies

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Guidance and support by our experienced and highly skilled team to choose the

best genetic test

Igenomix Genetic Counseling session

Doctors/PatientsReceive the genetic kit

Specific Kit will be sent along with the requisition and consent form to be signed

Sample collection:Blood, extracted DNA or tissuesample

Our Logistic and customer support team will scheduled the sample pick up and shipment

Sequencing and analysis is done100% In-House

Igenomix performTesting andAnalysis

Our International highly experienced scientific committee review and double check all cases

Samples shippedto Igenomix

Testing reportgeneration

The processHow does it work?

Peripheral blood EDTA vacutainer 20-25ºC 3 – 4 ml

A minimum 1 microgramof DNA at a concentrationof 50-100ng/µl

3 – 4 mm POC specimen or 50 100 mg of each tissue

10-15ml

300-500mg

20-25ºC

20-25ºC

20-25ºC

2-8 ºC

In a sealed Eppendorf tube

Sterile container

Sterile container with culture mediumor saline solution with 1% antibiotic

Tissue in sterile containerin saline and cardiac or cord blood in vacutainer

Purified genomicDNA

POC (fetal tissue)

Amniotic Fluid

Chorionic villi

Sample type Container Transportation Temperature Volume

Start a new success story with our

Contact our Genetic Counselors andGeneticists to get guidance and support

Certified Genetic Counselors to guide youand your patients in choosingthe right genetic testing.

Start a New success story with our

+91 11 665 17 800

Genetic Counseling Service

GET COUNSELED

TODAY

www.igenomix.co.inL-7, First floor, Green Park extension,

Pin 110016, New Delhi, INDIA

Phone +91 1166517800Email: info.india@igenomix.com