pre_natal - Middle East

Prenatal Screening
Analysis

using Non-invasive prenatal test (NIPT)

To Screen the Fetus Chromosomal abnormalities before the delivery through a non invasive technique

Non-invasive prenatal test
( NACE 5 , NACE 24, NACE 24 extended)

Non-invasive prenatal screening helps to avoid unnecessary amniocentesisNACE is a non-invasive prenatal screening test for the most frequent chromosomal abnormalities. The test is non-invasive, meaning that there is no risk to the fetus.

Prenatal Diagnostic/ Miscarriage
Analysis Analysis

using invasive prenatal test Using products of

CVS and Amniocentesis conception Amniocentesis

To Confirm if the Fetus is affected by
a genetic disorder or has
chromosomal abnormalities

Next Generation Sequencing
(CMA - Karyotyping
FISH - Precision panel - single Gene)

Single gene testing with Igenomix includes the possibility to individually analyse single genes that are that are associated with a clinical phenotype using next generation sequencing.

Whole Exome
Sequencing-Diagnostic.

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

Multiplex ligation dependent probe amplification

Multiplex Ligation dependent Probe Amplification (MLPA) is a multiplex PCR method used to detect abnormal copy numbers of up to 50 different genomic DNA or RNA sequences.

Expansions

Repeat expansions are common genetic variations that are usually associated to neurogenetic disorders. These expansions are a different class of genetic disease that occur due to dynamic mutations that can change from generation to generation.

Sanger/MiniSeq
Sequencing

Single gene testing with Igenomix includes the possibility to individually analyse single genes that are that are associated with a specific clinical phenotype using different techniques including sanger sequencing.