{"id":2851,"date":"2022-12-28T09:06:48","date_gmt":"2022-12-28T08:06:48","guid":{"rendered":"https:\/\/trisomytest.sk\/?page_id=2851"},"modified":"2023-01-30T09:16:40","modified_gmt":"2023-01-30T08:16:40","slug":"trisomy-test-complete-cysticka-fibroza","status":"publish","type":"page","link":"https:\/\/trisomytest.sk\/hu\/trisomy-test-complete-cysticka-fibroza\/","title":{"rendered":"TRISOMY test Complete +Ciszt\u00e1s fibr\u00f3zis"},"content":{"rendered":"

TRISOMY\u00a0Teljes teszt <\/strong><\/p>\n<\/div><\/div>

+Ciszt\u00e1s fibr\u00f3zis<\/p>\n<\/div><\/div>

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

A TRISOMY<\/strong> Teljes teszt\u00a0<\/strong>+Ciszt\u00e1s fibr\u00f3zis <\/strong>– egy kieg\u00e9sz\u00edt\u0151 vizsg\u00e1lat, amely a TRISOMY Teljes teszt mell\u00e9 rendelhet\u0151. Ez egy kiterjesztett vizsg\u00e1lat a CFTR g\u00e9n leggyakoribb F508del mut\u00e1ci\u00f3j\u00e1nak kimutat\u00e1s\u00e1ra, amely a ciszt\u00e1s fibr\u00f3zist okozza, amely az egyik leggyakoribb s\u00falyos \u00f6r\u00f6kletes betegs\u00e9g. A 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>

590 \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 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 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.
\nMinimaliz\u00e1lja az amniocent\u00e9zis (magzatv\u00edz invaz\u00edv mintav\u00e9tele) sz\u00fcks\u00e9gess\u00e9g\u00e9t.<\/p>\n<\/div><\/div><\/div><\/div>

Az F508del mut\u00e1ci\u00f3 jelenl\u00e9te a CFTR g\u00e9nben, amely a leggyakoribb ciszt\u00e1s fibr\u00f3zist okoz\u00f3 mut\u00e1ci\u00f3 a kauk\u00e1zusi popul\u00e1ci\u00f3ban.<\/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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A TRISOMY<\/strong> Teljes tesztet<\/strong> +Ciszt\u00e1s fibr\u00f3zis-t 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>