Array CGH: The latest innovation for increasing the chance of having a healthy baby

ArrayCGH (Array-based comparative genomic hybridization) is the latest medical technology that detects chromosomal abnormalities and analyzes all 23 pairs of chromosomes. It is also able to detect microdeletion and the missing or extra chromosomes and is used to analyze various genetic diseases or disorders. This is the only technique that can detect microdeletion.

Before implantation

This test detects the complete makeup of all 23 pairs of chromosomes in the embryo. The embryo that is the healthiest and contains all chromosomes are selected and transferred to the womb.

Benefits

• Increases success rate of IVF treatment
• Minimizes incidence of miscarriages
• Provides reassurance that a chromosome number problem does not exist in pregnancy

Suitable for

• Couples who are undergoing IVF treatment
• Pregnant women between the ages of 35-38 years
• Couples who have more than 2 failed IVF attempts
• Women who have had more than 3 miscarriages or miscarriages without any explanation

An amniocentesis is done to detect any micro deletion and missing chromosomes to locate genetic abnormalities

Benefits

• Detects more than 100 genetic abnormalities
• Reduces likelihood of chromosomal birth defects such as Down’s Syndrome

Suitable for

• Couples who concern microdeletion in their child
• Couples with a family history or those with a child suffering from a genetic disorder
• Couples who want to be reassured that their child is free from certain types of birth defects and genetic diseases

“Parents today must recognize the importance of preventing various genetic disorders. I recommend consultation with experienced physicians to select the right technology in undergoing various health tests, depending on each individual’s circumstances.”