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Genes2Me Pvt. Ltd.
www.genes2me.com
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SAS Tower-B, 1105, Medicity
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Microarray – An Advanced Chromosomal Testing
Microarray testing in pregnancy is used to detect chromosomal abnormality in the unborn child. It is also useful for individuals who do not fit in a specifically known syndrome such as Down syndrome or other abnormalities such as Developmental delay.

BriefingWire.com, 1/12/2022 - Microarray uses CGH (Comparative genomic hybridization) and SNP (Single nucleotide polymorphism) technology to screen and analyze chromosomal abnormality. Genes2Me offers CMA ( [FURL=https://www.genes2me.com/service/mother-and-child-care/chromosomal-microarray-analysis/microarray-analysis]chromosomal microarray analysis[/FURL]) that helps in fetal screening for identifying copy number variants. It helps detect underlying genetic conditions like autism, developmental delay, and predisposition to congenital disease.

Genetic Testing for Identifying Chromosomal Abnormality

Genes2Me offers comprehensive genetic testing using Microarray Technology to analyze micro-duplication or micro-deletion across genomic information. The gain and loss are called copy number variants (CNVs), causing genetic conditions or related symptoms. The robust [FURL=https://genes2me.com/personalized-health/genes2fit]genetic testing[/FURL] and screening method plays a crucial role in detecting abnormalities due to variations like missing or extra chromosomal material.

Genes2Me has made the entire process easy, streamlined, and affordable, supported by pre and post genetic counselling. The first line testing method detects hundreds of genetic conditions and provides a preventive intervention. The test is made convenient with the help of extraction of blood samples and analysis of other samples like AF, CVS, POC, buccal swab etc.

Detection of Developmental Disabilities and Congenital Anomalies

[FURL=https://genes2me.com/blog/index.php/2022/01/08/important-facts-to-know-about-chromosomal-microarray-test/]Chromosomal Microarray[/FURL] is an essential clinical diagnostic test suitable for genetic testing in individuals with unexplained development delay, autism spectrum disorders, congenital anomalies, and intellectual disability. Microarray technology provides early diagnosis and intervention through highly sensitive and accurate screening of the copy number variants. Genes2Me offers advanced chromosomal Microarray as a frontline diagnostic and screening method for analyzing development delays in children.

The high-resolution testing and screening method accurately detect the microscopic aberrations or changes in the chromosome. It helps identify micro-deletion, micro-duplication, or chromosomal aberrations such as unbalanced translocation resulting in recurring pregnancy loss, pre-natal aneuploidies which can predispose fetus to certain [FURL=https://genes2me.com/personalized-health/genes2health]genetic disorders[/FURL]. The technology is constantly upgraded to provide an affordable intervention to genetic disease or its predisposition.

With fast and rapid screening and accuracy of the report generation, licensed and certified genetic counsellors offer complete diagnostics and genetic counselling. The affordable genetic screening through Microarray has helped analyze the chromosomal abnormality and detection of aneuploidy, helping with genetic interventions. [FURL=https://genes2me.com/service/]Genes2Me[/FURL] offer complete guidance and genetic counselling for individuals screened positive for genetic abnormality to streamline further interventions.

 
 
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