Karyomapping · is an embryo examination before transfer. There Is a complex technique, a technology for finding genetic abnormalities to check if the embryo has abnormal genes or not.

Dna sample Will be screened initially by DNA tests from parents Or relatives with unusual characteristics, Preliminary testing of those samples using Karyomapping allows DNA testing to find disfunction genes.

Karyomapping also provides information on the entire genome, which means we can identify certain chromosomal errors that cause embryo transfer and miscarriage failure. It has the potential to help us identify the strongest and most likely embryos in a successful pregnancy, which we expect that will help to improve birth rates for our patient

The benefits of Karyomapping that we can take the DNA sample from parents and patients By examining the characteristics of DNA, comparing it, then draw a chart showing what the genetic path is, and analyze whether the baby is genetically transferred, including chromosomal abnormalities

Karyomapping Can detect the diseases caused by abnormal single gene such as

• Alzheimer's disease
• Cystic Fibrosis
• Thalassemia
• Duchenne muscular dystrophy
• abnormalities of sex chromosome
• BRCA1 / BRCA2(Genetic diseases, Ovary cancer)
• PGD tests can find clear results in a single gene abnormality. Despite some genetic diseases that can be seen from all genetics In cases like this To detect a single gene using PGD, a kayomapping technique is needed to help solve the problem

·STORK is a hospital with karyomapping. The karyomapping is DNA sample comparison · of parents and relatives And finding chromosome abnormalities by drawing a chart At the same time can analyze the position SNP · more than Thirty thousand positions For quick checking From embryo DNA testing and comparison of SNP. we can select embryos without genetic diseases