{"id":2758,"date":"2023-01-20T10:33:23","date_gmt":"2023-01-20T09:33:23","guid":{"rendered":"https:\/\/trisomytest.sk\/?page_id=2758"},"modified":"2023-01-20T10:33:23","modified_gmt":"2023-01-20T09:33:23","slug":"trisomy-test-2","status":"publish","type":"page","link":"https:\/\/trisomytest.sk\/cs\/trisomy-test-2\/","title":{"rendered":"Trisomy test +"},"content":{"rendered":"

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

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

TRISOMY<\/strong> test +<\/strong> je nadstavbov\u00e9 genetick\u00e9 laborat\u00f3rne vy\u0161etrenie, ktor\u00e9 dok\u00e1\u017ee odhali\u0165 viac chromoz\u00f3mov\u00fdch por\u00fach v porovnan\u00ed s TRISOMY testom a testom TRISOMY test XY. Zis\u0165uje riziko triz\u00f3mie chromoz\u00f3mov 21, 18 a 13, poruchy po\u010dtu pohlavn\u00fdch chromoz\u00f3mov a vybran\u00fdch mikrodel\u00e9ci\u00ed chromoz\u00f3mov, pri ktor\u00fdch ch\u00fdba \u010das\u0165 niektor\u00e9ho chromoz\u00f3mu. TRISOMY test + stanovuje aj chromoz\u00f3mov\u00e9 pohlavie plodu. Pred objednan\u00edm testu je potrebn\u00e9 obozn\u00e1mi\u0165 sa s aktu\u00e1lnym Pou\u010den\u00edm o genetickom laborat\u00f3rnom vy\u0161etren\u00ed.<\/p>\n<\/div><\/div><\/div><\/div>

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

Vyl\u00fa\u010di \u010dast\u00e9 poruchy po\u010dtu chromoz\u00f3mov plodu 21, 18 a 13 (pr\u00ed\u010dina Downovho, Edwardsovho a Patauovho syndr\u00f3mu).<\/p>\n<\/div><\/div><\/div><\/div>

Vyl\u00fa\u010di mo\u017en\u00e9 aber\u00e1cie po\u010dtu pohlavn\u00fdch chromoz\u00f3mov (pr\u00ed\u010dina Turnerovho syndr\u00f3mu 45,X; Klinefelterovho syndr\u00f3mu XXY a Syndr\u00f3mov XYY a XXX).<\/p>\n<\/div><\/div><\/div><\/div>

Vyl\u00fa\u010di mo\u017en\u00e9 vybran\u00e9 chromoz\u00f3mov\u00e9 del\u00e9cie (pr\u00ed\u010dina DiGeorgeov syndr\u00f3m 22q11, Syndr\u00f3m del\u00e9cie 1p36, Praderov-Williho a Angelmanov syndr\u00f3m, Cri-du-chat syndr\u00f3m, Wolfov-Hirschhornov syndr\u00f3m).<\/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 test +<\/span><\/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>