{"id":2762,"date":"2023-01-20T10:35:58","date_gmt":"2023-01-20T09:35:58","guid":{"rendered":"https:\/\/trisomytest.sk\/?page_id=2762"},"modified":"2023-01-20T10:35:58","modified_gmt":"2023-01-20T09:35:58","slug":"proc-si-vybrat-trisomy","status":"publish","type":"page","link":"https:\/\/trisomytest.sk\/cs\/proc-si-vybrat-trisomy\/","title":{"rendered":"Pro\u010d si vybrat TRISOMY"},"content":{"rendered":"

Pre\u010do si vybra\u0165 TRISOMY<\/strong>?<\/p>\n<\/div><\/div>

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Unik\u00e1tny<\/b><\/p>\n<\/div><\/div>

Dok\u00e1\u017ee analyzova\u0165 naj\u0161ir\u0161iu \u0161k\u00e1lu chromoz\u00f3mov\u00fdch por\u00fach plodu naprie\u010d cel\u00fdm gen\u00f3mom u\u017e od 11. t\u00fd\u017ed\u0148a tehotenstva.<\/p>\n<\/div><\/div><\/div><\/div>

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Spo\u013eahliv\u00fd<\/b><\/p>\n<\/div><\/div>

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Viac ako 99,93 % spo\u013eahlivos\u0165 v detekcii naj\u010dastej\u0161\u00edch chromoz\u00f3mov\u00fdch por\u00fach plodu potvrden\u00e1 v \u0161t\u00fadii realizovanej na 7 279 vzork\u00e1ch tehotn\u00fdch \u017eien.<\/p>\n

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Sekelska M, Izsakova A, Kubosova K, Tilandyova P, Csekes E, Kuchova Z, Hyblova M, Harsanyova M, Kucharik M, Budis J, Szemes T, Minarik G. Result of Prospective Validation of the Trisomy Test\u00ae for the Detection of Chromosomal Trisomies. Diagnostics (Basel). 2019 Oct 2;9(4):138.<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div><\/div><\/div><\/div>
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Komplexn\u00fd<\/strong><\/p>\n<\/div><\/div>

Poskytuje detailn\u00fd skr\u00edning DNA plodu a z\u00e1rove\u0148 bezplatn\u00e9 overenie pozit\u00edvneho v\u00fdsledku vy\u0161etren\u00edm plodovej vody testom GenomeScreen prenatal.<\/p>\n<\/div><\/div><\/div><\/div><\/div>

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Bezbolestn\u00fd<\/strong><\/p>\n<\/div><\/div>

Vy\u0161etrenie z krvi matky.<\/p>\n<\/div><\/div><\/div><\/div>

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R\u00fdchly<\/strong><\/p>\n<\/div><\/div>

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V\u00fdsledok dostupn\u00fd do 5 pracovn\u00fdch dn\u00ed.<\/p>\n

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Za predpokladu, \u017ee vzorku bolo mo\u017en\u00e9 laborat\u00f3rne spracova\u0165 v s\u00falade so spr\u00e1vnou laborat\u00f3rnou praxou, a bolo mo\u017en\u00e9 z\u00edska\u0165 v\u00fdsledok, ktor\u00fd na \u00farovni rozli\u0161ovacej schopnosti pou\u017eitej met\u00f3dy odpoved\u00e1 na skr\u00edningov\u00fa alebo diagnostick\u00fa ot\u00e1zku, laborat\u00f3rium vyd\u00e1 v\u00fdsledok testu zvy\u010dajne do 5 pracovn\u00fdch dn\u00ed, alebo asi u 10 % vzoriek do 8 pracovn\u00fdch dn\u00ed (z d\u00f4vodu biologickej variability a neo\u010dak\u00e1van\u00fdch technick\u00fdch pr\u00ed\u010din s\u00favisiacich s analyzovanou vzorkou).
\nLehota 5 resp. 8 pracovn\u00fdch dn\u00ed sa po\u010d\u00edta odo d\u0148a nasleduj\u00faceho po doru\u010den\u00ed vzorky do Laborat\u00f3ria alebo d\u0148a identifikovania platby za test (pod\u013ea toho \u010do nastane nesk\u00f4r).<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div><\/div><\/div><\/div>
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Bezpe\u010dn\u00fd<\/strong><\/p>\n<\/div><\/div>

Bez rizika pre plod.<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/section>

Bezpe\u010dnos\u0165 testu<\/h3>\n<\/div><\/div>

TRISOMY test je neinvaz\u00edvne skr\u00edningov\u00e9 vy\u0161etrenie z krvi matky, ktor\u00e9 dok\u00e1\u017ee s ve\u013ekou presnos\u0165ou vyl\u00fa\u010di\u0165 pr\u00edtomnos\u0165 chromoz\u00f3mov\u00fdch por\u00fach plodu u\u017e od 11. t\u00fd\u017ed\u0148a gravidity. V krvi matky koluje u\u017e v ranom \u0161t\u00e1diu tehotenstva DNA plodu. Pomocou genetick\u00e9ho vy\u0161etrenia v laborat\u00f3ri\u00e1ch je mo\u017en\u00e9 DNA plodu izolova\u0165, analyzova\u0165 a identifikova\u0165 pr\u00edpadn\u00fd v\u00fdskyt aneuploidi\u00ed a aber\u00e1ci\u00ed chromoz\u00f3mov.<\/p>\n<\/div><\/div><\/div><\/div>

V porovnan\u00ed s in\u00fdmi skr\u00edningov\u00fdmi met\u00f3dami:<\/strong><\/p>\n<\/div><\/div>