{"id":2760,"date":"2023-01-20T10:33:27","date_gmt":"2023-01-20T09:33:27","guid":{"rendered":"https:\/\/trisomytest.sk\/?page_id=2760"},"modified":"2023-01-20T10:33:27","modified_gmt":"2023-01-20T09:33:27","slug":"trisomy-test-complete","status":"publish","type":"page","link":"https:\/\/trisomytest.sk\/cs\/trisomy-test-complete\/","title":{"rendered":"TRISOMY test Complete"},"content":{"rendered":"

TRISOMY test Complete<\/strong><\/p>\n<\/div><\/div>

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O teste<\/h3>\n<\/div><\/div>

TRISOMY<\/strong> test Complete<\/strong>\u00a0je komplexn\u00fd NIPT – Neinvaz\u00edvny prenat\u00e1lny skr\u00edningov\u00fd test pre v\u0161etk\u00fdch 23 p\u00e1rov chromoz\u00f3mov, ktor\u00fd spo\u013eahlivo odhal\u00ed chromoz\u00f3mov\u00e9 poruchy naprie\u010d cel\u00fdm gen\u00f3mom plodu u\u017e od 11. t\u00fd\u017ed\u0148a tehotenstva. Test 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. Pred objednan\u00edm testu je potrebn\u00e9 obozn\u00e1mi\u0165 sa s aktu\u00e1lnym Pou\u010den\u00edm o genetickom laborat\u00f3rnom vy\u0161etren\u00ed<\/a><\/span>.<\/p>\n<\/div><\/div><\/div><\/div>

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chromoz\u00f3mov\u00e9 poruchy<\/span><\/i><\/a><\/div>
dedi\u010dn\u00e9 ochorenia<\/span><\/i><\/a><\/div><\/div>

\u010co odhal\u00ed?<\/p>\n<\/div><\/div>

V\u010faka detailnej anal\u00fdze DNA plodu odhal\u00ed poruchy v po\u010detnosti a mno\u017estve genetick\u00e9ho materi\u00e1lu v\u0161etk\u00fdch 23 p\u00e1rov chromoz\u00f3mov, a to ako na celochromoz\u00f3movej tak aj subchromoz\u00f3movej \u00farovni.<\/p>\n<\/div><\/div><\/div><\/div>

Okrem naj\u010dastej\u0161\u00edch triz\u00f3mi\u00ed chromoz\u00f3mov 21, 18, 13 odhal\u00ed aj tzv. zriedkav\u00e9 zmeny po\u010dtu ktor\u00e9hoko\u013evek z chromoz\u00f3mov vr\u00e1tane pohlavn\u00fdch, ktor\u00e9 m\u00f4\u017eu by\u0165 spojen\u00e9 s mo\u017en\u00fdmi komplik\u00e1ciami po\u010das tehotenstva.<\/p>\n<\/div><\/div><\/div><\/div>

Test dok\u00e1\u017ee odhali\u0165 del\u00e9cie a duplik\u00e1cie, ktor\u00e9 s\u00fa v\u00e4\u010d\u0161inou spojen\u00e9 s klinicky relevantn\u00fdmi poruchami plodu. Tie nie je mo\u017en\u00e9 odhali\u0165 in\u00fdmi be\u017ene vyu\u017e\u00edvan\u00fdmi met\u00f3dami prenat\u00e1lneho skr\u00edningu.<\/p>\n<\/div><\/div><\/div><\/div><\/div>

Odhal\u00ed mo\u017en\u00e9 falo\u0161ne pozit\u00edvne v\u00fdsledky biochemick\u00e9ho prenat\u00e1lneho skr\u00edningu.<\/p>\n<\/div><\/div><\/div><\/div>

Minimalizuje nutnos\u0165 absolvova\u0165 amniocent\u00e9zu (invaz\u00edvny odber plodovej vody).<\/p>\n<\/div><\/div><\/div><\/div>

V pr\u00edpade z\u00e1ujmu ur\u010d\u00ed pohlavie plodu.<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/section>

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TRISOMY<\/strong> test Complete<\/strong> m\u00f4\u017ee absolvova\u0165 tehotn\u00e1 \u017eena na vlastn\u00fa \u017eiados\u0165 a po genetickej konzult\u00e1cii. Je vhodn\u00fd pre ka\u017ed\u00fa \u017eenu od 11. t\u00fd\u017ed\u0148a tehotenstva, ak:<\/p>\n<\/div><\/div>