{"id":33752,"date":"2022-11-26T11:01:49","date_gmt":"2022-11-26T11:01:49","guid":{"rendered":"https:\/\/gyncentrum.pl\/diagnostyka-preimplantacyjna\/karyomapping\/"},"modified":"2024-02-21T10:25:20","modified_gmt":"2024-02-21T10:25:20","slug":"karyomapping","status":"publish","type":"servies","link":"https:\/\/gyncentrum.pl\/en\/preimplantation-diagnosis\/karyomapping\/","title":{"rendered":"Karyomapping"},"content":{"rendered":"\n
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Karyomapping <\/h1>\n
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\n \n \n Home<\/a>\n \"\"\n \n Preimplantation diagnosis<\/a>\n \n Karyomapping<\/span>\n <\/span>\n <\/span>\n <\/span>\n <\/div>\n\n \n\n\n
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\n \"\"\n <\/div>\n PREIMPLANTATION DIAGNOSIS<\/span>\n\n <\/div>\n

Reduces the risk of transmitting monogenic disease to the embryo.<\/p>\n<\/h3>\n

Preimplantation genetic testing for monogenic diseases (PGT-M) reduces the risk of transmitting a specific genetic disease to a child, thereby increasing the chance of a successful IVF procedure and the birth of a healthy baby. One of the most advanced systems for indirect identification of defects in single genes is PGT-M by karyomapping.<\/strong> Gyncentrum Genetic Laboratory is the first and only laboratory in Poland to use it.<\/p>\n

AtGyncentrum Genetic Laboratory, in addition to karyomapping, we also perform other preimplantation genetic tests, including: PGT-A, niPGT-A, PGT-M and PGT-SR. <\/strong><\/p>\n<\/div>\n \n \n Make an appointment for a consultation<\/span>\n\n <\/a>\n \n <\/div>\n

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Get the chance to have a healthy baby!
\nMake an appointment for a consultation with a Gyncentrum infertility treatment specialist<\/strong><\/p>\n<\/h3>\n

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\n ABOUT THE STUDY <\/span>\n

What is karyomapping?<\/p>\n<\/h2>\n

Karyomapping, or so-called karyomapping, is a new technique for genetic diagnosis of embryos prior to their transfer into the uterus. Thanks to it, couples using the IVF procedure can avoid passing on to future offspring a mutation in a single gene they carry.<\/strong><\/p>\n

Karyomapping checks for about 300,000 single nucleotide polymorphisms (SNPs, or single n<\/em>ucleotide polymorphisms), i.e. changes within the basic components of human DNA. Each nucleotide is designated by a letter symbol A, T, C, G. Arranged in the correct order, the nucleotides form nucleotide sequences. These, in turn, determine the order of the 20 amino acids that make up proteins. Sometimes, however, a mistake will occur within a given sequence and a letter is replaced by another. Single nucleotide polymorphisms are just such “typos,” and karyomapping by identifying them allows us to detect monogenic disease. Using karyomapping, we can examine maternal, paternal or other family members’ chromosomes and, based on this, create a DNA “fingerprint” of the chromosome where the mutated gene is located.<\/strong><\/p>\n<\/span>\n \n \n Make an appointment<\/span>\n\n <\/a>\n <\/div>\n

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