Prenatal & Maternal Diagnostics
DNA Labs India | Diagnostic Tests
Prenatal & Maternal Diagnostics
Clinical Overview
Sub-category mapping under Genetics & Genomics
| Reviewed by: Dr. Rajesh Kumar, MD Pathology | ISO 9001:2015 Certified Laboratory
This content is for educational purposes only. Always consult a qualified healthcare provider for medical advice.
Tests
Chromosome Analysis Products of Conception Reflex Testing to FISH for Aneuploidy Detection Test
The purpose of this test is to detect aneuploidy in products of conception to determine the genetic...
Chromosome Analysis Cord Blood Test
To identify chromosomal abnormalities in newborns for early diagnosis and management of genetic diso...
Chromotouch Chromosome SNP Microarray Optima Products of Conception Test
The primary purpose of the Chromotouch Chromosome SNP Microarray Optima POC Test is to determine whe...
FISH - Amnio Three Probes: Trisomy 18 X & Y Test
The purpose of this test is to provide rapid prenatal diagnosis for trisomy 18 and sex chromosome ab...
FISH - Amnio Two Probes: Trisomy 13 & 21 Test
To be used as a prenatal screen, in conjunction with full chromosome analysis, to detect aneuploidy...
FISH - SRY Gene Test
The primary purpose of the FISH SRY Gene Test is to detect deletions or abnormalities of the SRY gen...
FISH - Trisomy 21 / Down Syndrome Test
The FISH - Trisomy 21 / Down Syndrome Test is performed to diagnose Down Syndrome in the fetus durin...
Preimplantation Genetic Screening (PGS) Test
This panel tests the following diseases using enzyme assay methodology on chorionic villus biopsy ti...
Prenatal Diagnosis Panel 1 Chorionic Villus Biopsy Test
This assay detects specific sulphate with qualitative analysis of their relative amounts, useful for...
Thalassemia Alpha Trio Prenatal Mutation Detection Test
The purpose of the Thalassemia Alpha Trio Prenatal Mutation Detection Test is to identify alpha thal...
NR1H4 Gene Intrahepatic cholestasis of pregnancy, NR1H4 related NGS Genetic Test
The purpose of the NR1H4 Gene NGS Genetic Test is to identify mutations in the NR1H4 gene associated...
Chromosomes 13, 18, 21, X & Y
The purpose of this test is to identify numerical abnormalities (aneuploidy) in chromosomes 13, 18,...
Microarray 60K (AF/CVS/CB) + Karyotyping + FISH chromosome 13,18,21, X and Y
To detect chromosomal abnormalities and genetic disorders through a combination of Microarray, Karyo...
Microarray 60K (AF/CVS) + Karyotyping
To diagnose chromosomal abnormalities and genetic disorders in prenatal settings, enabling early int...
Microarray 60K (AF/CVS) + Karyotyping + FISH chromosome 21
To diagnose chromosomal abnormalities such as Down syndrome (trisomy 21), other aneuploidies, copy n...
Microarray 60K (AF/CVS/CB)
The purpose of the Microarray 60K (AF/CVS/CB) test is to diagnose genetic disorders and chromosomal...
Microarray 750K (AF/CVS/CB/POC/PB)
The primary purpose of the Microarray 750K test is to identify genetic abnormalities that may be cau...
Prenatal Diagnostic Screening by Karyotyping
To detect chromosomal abnormalities in the fetus, such as aneuploidy or structural defects, for earl...
Prenatal Alpha Thalassemia Mutation Screening (3 Common Mutation)
The purpose of this test is to identify whether a fetus has inherited alpha thalassemia mutations fr...
Prenatal Diagnostic Screening by Karyotyping + FISH (for any one 13, 18, 21, X and Y)
The purpose of this test is to detect chromosomal abnormalities in the fetus, such as trisomy 21 (Do...
QF PCR [Any One Marker]+ Karyotyping
The purpose of QF PCR [Any One Marker]+ Karyotyping is to diagnose genetic conditions by detecting c...
Prenatal Hemophilia A Common Mutation Screening (Factor VIII Intron 22 and Intron 1 Inversion Analysis)
The purpose of this test is to screen for common mutations causing Hemophilia A in fetuses, enabling...
QF PCR Panel [13,18,21,XY]
The purpose of the QF PCR Panel [13,18,21,XY] is to rapidly and accurately detect common chromosomal...
QF PCR Panel [13,18,21,XY] + Karyotyping
To diagnose chromosomal abnormalities that can cause developmental issues, birth defects, and reprod...
Chromosome Analysis Amniotic Fluid Test
The test is recommended between 15 and 20 weeks of gestation to identify numerical and structural ch...
Chromotouch Chromosome SNP Microarray Optima Prenatal Test
This test is performed to detect fetal chromosomal abnormalities including aneuploidies, microdeleti...
Sickle Cell Anemia Trio Prenatal Mutation Detection Test
The purpose of this test is to detect HBB gene mutations linked to sickle cell anemia in the fetus u...
Beta Thalassemia-HBB Full Gene Analysis (Couple + Prenatal) [Trio Analysis]
The primary purpose of this test is to identify mutations in the HBB gene in both parents and the fe...
Cystic Fibrosis Mutation Screening (CFTR - Del 508)[Prenatal]
The purpose of this prenatal test is to determine whether the fetus has inherited the F508del mutati...
DMD Mutation Screening (79 Exons) [Prenatal]
The primary purpose of this prenatal test is to determine whether the fetus has inherited a pathogen...
Maternal Cell Contamination
The purpose of the Maternal Cell Contamination test is to detect the presence of maternal cells in a...
FISH - Trisomy 13 / Patau Syndrome Test
The primary purpose of the FISH Trisomy 13 test is to confirm or rule out the presence of an extra c...
FISH - Trisomy 18 / Edward Syndrome Test
The primary purpose of the FISH Trisomy 18 test is to confirm or rule out the presence of an extra c...
FISH for Pre or Postnatal Diagnosis Chromosome 13 21
The primary purpose of this FISH test is to detect aneuploidy (abnormal number of chromosomes) for c...
FISH for Pre or Postnatal Diagnosis Chromosome 18, X Y
The primary purpose of this FISH test is to detect numerical abnormalities (aneuploidy) of chromosom...
FISH for Pre or Postnatal Diagnosis Chromosome 13 22
The primary purpose of FISH for chromosomes 13 and 22 is to detect numerical abnormalities (aneuploi...
FISH for Pre or Postnatal Diagnosis Chromosome 13 23
The primary purpose of FISH for chromosomes 13 and 23 is to detect aneuploidies (abnormal number of...
NIPT Advanced for 23 Chromosomes
The primary purpose of the NIPT Advanced for 23 Chromosomes test is to screen for fetal chromosomal...
Maternal Cell Contamination MCC Test
The primary purpose of the MCC test is to verify that a DNA sample collected for genetic analysis is...