{"id":2850,"date":"2022-11-03T10:00:15","date_gmt":"2022-11-03T09:00:15","guid":{"rendered":"https:\/\/trisomytest.sk\/?page_id=2850"},"modified":"2025-12-09T10:59:28","modified_gmt":"2025-12-09T09:59:28","slug":"trisomy-test-complete","status":"publish","type":"page","link":"https:\/\/trisomytest.sk\/hu\/trisomy-test-complete\/","title":{"rendered":"TRISOMY test Complete"},"content":{"rendered":"

TRISOMY Teljes teszt<\/strong><\/p>\n<\/div><\/div>

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A tesztr\u0151l<\/h3>\n<\/div><\/div>

A TRISOMY<\/strong> Teljes teszt<\/strong> egy \u00e1tfog\u00f3 non-invaz\u00edv prenat\u00e1lis sz\u0171r\u0151vizsg\u00e1lat (NIPT) mind a 23 kromosz\u00f3map\u00e1rra, amely megb\u00edzhat\u00f3an kimutatja a kromosz\u00f3ma rendelleness\u00e9geket a teljes magzati genomban a terhess\u00e9g 11. het\u00e9t\u0151l kezdve. A teszt a magzat r\u00e9szletes DNS-sz\u0171r\u00e9s\u00e9t, \u00e9s egyben a pozit\u00edv eredm\u00e9ny ingyenes igazol\u00e1s\u00e1t magzatv\u00edz vizsg\u00e1lat\u00e1val a GenomeScreen prenat\u00e1lis teszttel.\u00a0A vizsg\u00e1lat megrendel\u00e9se el\u0151tt meg kell ismerni az aktu\u00e1lis Genetikai laborat\u00f3riumi vizsg\u00e1lati t\u00e1j\u00e9koztat\u00f3t<\/a><\/span>.<\/p>\n<\/div><\/div><\/div><\/div>

A vizsg\u00e1lat \u00e1ra<\/p>\n<\/div><\/div>

530 \u20ac<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div>

kromosz\u00f3ma rendelleness\u00e9gek<\/span><\/i><\/a><\/div>
\u00f6r\u00f6kletes betegs\u00e9gek<\/span><\/i><\/a><\/div><\/div>

Mit fog kimutatni?<\/p>\n<\/div><\/div>

A magzat DNS-\u00e9nek r\u00e9szletes elemz\u00e9s\u00e9nek k\u00f6sz\u00f6nhet\u0151en mind a 23 kromosz\u00f3map\u00e1r genetikai anyag\u00e1nak gyakoris\u00e1g\u00e1ban \u00e9s mennyis\u00e9g\u00e9ben rendelleness\u00e9geket t\u00e1r fel, mind a teljes kromosz\u00f3ma, mind a szubkromosz\u00f3ma szintj\u00e9n.<\/p>\n<\/div><\/div><\/div><\/div>

A 21-es, 18-as, 13-as kromosz\u00f3m\u00e1k leggyakoribb trisz\u00f3mi\u00e1in t\u00falmen\u0151en a kromosz\u00f3m\u00e1k, k\u00f6zt\u00fck a nemi kromosz\u00f3m\u00e1k sz\u00e1m\u00e1nak \u00fagynevezett ritka elv\u00e1ltoz\u00e1sait is felt\u00e1rja, amelyek a terhess\u00e9g alatti esetleges sz\u00f6v\u0151dm\u00e9nyekkel j\u00e1rhatnak.<\/p>\n<\/div><\/div><\/div><\/div>

A teszt k\u00e9pes kimutatni a del\u00e9ci\u00f3kat \u00e9s a duplik\u00e1ci\u00f3kat, amelyek t\u00f6bbnyire klinikailag jelent\u0151s magzati rendelleness\u00e9gekhez kapcsol\u00f3dnak. Ezek m\u00e1s, \u00e1ltal\u00e1nosan haszn\u00e1lt prenat\u00e1lis sz\u0171r\u00e9si m\u00f3dszerekkel nem mutathat\u00f3k ki.<\/p>\n<\/div><\/div><\/div><\/div><\/div>

Kimutatja a biok\u00e9miai prenat\u00e1lis sz\u0171r\u00e9s esetleges hamis pozit\u00edv eredm\u00e9nyeit.<\/p>\n<\/div><\/div><\/div><\/div>

Minimaliz\u00e1lja az amniocent\u00e9zis (magzatv\u00edz invaz\u00edv mintav\u00e9tele) sz\u00fcks\u00e9gess\u00e9g\u00e9t.<\/p>\n<\/div><\/div><\/div><\/div>

\u00c9rdekl\u0151d\u00e9s eset\u00e9n meghat\u00e1rozza a magzat nem\u00e9t.<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/section>

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TRISOMY<\/strong> Teljes tesztet<\/strong> a terhes n\u0151 saj\u00e1t k\u00e9r\u00e9s\u00e9re \u00e9s genetikai konzult\u00e1ci\u00f3t k\u00f6vet\u0151en is elv\u00e9geztetheti. A terhess\u00e9g 11. het\u00e9t\u0151l minden n\u0151 sz\u00e1m\u00e1ra alkalmas, ha:<\/p>\n<\/div><\/div>