{"id":1233,"date":"2016-05-22T05:15:38","date_gmt":"2016-05-22T05:15:38","guid":{"rendered":"https:\/\/www.primarycaregenetics.org\/?page_id=1233"},"modified":"2018-02-16T13:05:29","modified_gmt":"2018-02-16T13:05:29","slug":"varovne-signaly","status":"publish","type":"page","link":"https:\/\/www.primarycaregenetics.org\/?page_id=1233&lang=cz","title":{"rendered":"Varovn\u00e9 sign\u00e1ly"},"content":{"rendered":"<p>Ur\u010dit\u00e9 znaky v\u00a0osobn\u00ed a rodinn\u00e9 anamn\u00e9ze zvy\u0161uj\u00ed pravd\u011bpodobnost d\u011bdi\u010dn\u00e9 p\u0159\u00ed\u010diny obt\u00ed\u017e\u00ed. Ty jsou naz\u00fdv\u00e1ny varovn\u00e9 sign\u00e1ly (red flags) a jejich p\u0159\u00edtomnost by m\u011bla klinika upozornit na zv\u00fd\u0161en\u00e9 riziko d\u011bdi\u010dn\u00e9 (tj. monogenn\u00ed nebo chromozom\u00e1ln\u00ed) p\u0159\u00ed\u010diny obt\u00ed\u017e\u00ed.<\/p>\n<p>Nap\u0159\u00edklad kdy\u017e v\u00e1m pacient polo\u017e\u00ed ot\u00e1zku ohledn\u011b mo\u017en\u00e9 d\u011bdi\u010dn\u00e9 p\u0159\u00ed\u010diny n\u00e1dorov\u00e9ho onemocn\u011bn\u00ed v\u00a0rodin\u011b, m\u011bli byste v\u011bd\u011bt, \u017ee k v\u00fdznamn\u00fdm indik\u00e1tor\u016fm zv\u00fd\u0161en\u00e9ho rizika pat\u0159\u00ed n\u00e1sleduj\u00edc\u00ed jevy:<\/p>\n<ul>\n<li>v\u00fdskyt n\u00e1dor\u016f v ni\u017e\u0161\u00edm v\u011bku, ne\u017e je obvykl\u00e9<\/li>\n<li>v\u00a0p\u0159\u00edpad\u011b d\u011bdi\u010dn\u00fdch n\u00e1dorov\u00fdch syndrom\u016f se vyskytuj\u00ed u pokrevn\u00edch p\u0159\u00edbuzn\u00fdch \u010dast\u011bji ur\u010dit\u00e9 typy n\u00e1dor\u016f (nap\u0159. rakovina prsu a vaje\u010dn\u00edk\u016f v\u00a0p\u0159\u00edpad\u011b heredit\u00e1rn\u00edho syndromu n\u00e1dor\u016f prsu a ov\u00e1ria, rakovina tlust\u00e9ho st\u0159eva a karcinom endometria u Lynchova syndromu, atd)<\/li>\n<li>v\u00fdskyt n\u011bkolik prim\u00e1rn\u00edch n\u00e1dor\u016f u jedn\u00e9 osoby<\/li>\n<li>neobvykl\u00e9 typy n\u00e1dor\u016f, jako nap\u0159. Ca prsu u mu\u017ee<\/li>\n<\/ul>\n<p>V ka\u017ed\u00e9m z na\u0161ich modul\u016f jsou pops\u00e1ny varovn\u00e9 sign\u00e1ly, s jejich\u017e pomoc\u00ed dok\u00e1\u017eete identifikovat pacienty se zv\u00fd\u0161en\u00fdm rizikem d\u011bdi\u010dn\u00e9 p\u0159\u00ed\u010diny obt\u00ed\u017e\u00ed.<\/p>\n<p>P\u0159ehled varovn\u00fdch sign\u00e1l\u016f pro obecnou klinickou praxi, pro n\u00e1dorov\u00e1 onemocn\u011bn\u00ed, pro kardiologick\u00e1 onemocn\u011bn\u00ed, pro podez\u0159en\u00ed na genetick\u00e9 onemocn\u011bn\u00ed u d\u00edt\u011bte a t\u00fdkaj\u00edc\u00ed se reprodukce a t\u011bhotenstv\u00ed jsou dostupn\u00e9 v\u00a0PDF form\u00e1tu v sekci Praktick\u00e9 n\u00e1stroje pro ka\u017edodenn\u00ed praxi <a href=\"https:\/\/www.primarycaregenetics.org\/?page_id=2160&amp;lang=cz\">zde<\/a>.<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Ur\u010dit\u00e9 znaky v\u00a0osobn\u00ed a rodinn\u00e9 anamn\u00e9ze zvy\u0161uj\u00ed pravd\u011bpodobnost d\u011bdi\u010dn\u00e9 p\u0159\u00ed\u010diny obt\u00ed\u017e\u00ed. Ty jsou naz\u00fdv\u00e1ny varovn\u00e9 sign\u00e1ly (red flags) a jejich p\u0159\u00edtomnost by m\u011bla klinika upozornit na zv\u00fd\u0161en\u00e9 riziko d\u011bdi\u010dn\u00e9 (tj. monogenn\u00ed nebo chromozom\u00e1ln\u00ed) p\u0159\u00ed\u010diny obt\u00ed\u017e\u00ed. Nap\u0159\u00edklad kdy\u017e v\u00e1m pacient polo\u017e\u00ed ot\u00e1zku ohledn\u011b mo\u017en\u00e9 d\u011bdi\u010dn\u00e9 p\u0159\u00ed\u010diny n\u00e1dorov\u00e9ho onemocn\u011bn\u00ed v\u00a0rodin\u011b, m\u011bli byste v\u011bd\u011bt, \u017ee k v\u00fdznamn\u00fdm indik\u00e1tor\u016fm zv\u00fd\u0161en\u00e9ho rizika pat\u0159\u00ed n\u00e1sleduj\u00edc\u00ed jevy: v\u00fdskyt n\u00e1dor\u016f v ni\u017e\u0161\u00edm v\u011bku, ne\u017e je obvykl\u00e9 v\u00a0p\u0159\u00edpad\u011b d\u011bdi\u010dn\u00fdch n\u00e1dorov\u00fdch syndrom\u016f se vyskytuj\u00ed u pokrevn\u00edch p\u0159\u00edbuzn\u00fdch \u010dast\u011bji ur\u010dit\u00e9 typy [&#8230;]<\/p>\n","protected":false},"author":3,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"template-fullwidth.php","meta":{"ngg_post_thumbnail":0},"_links":{"self":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages\/1233"}],"collection":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=1233"}],"version-history":[{"count":10,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages\/1233\/revisions"}],"predecessor-version":[{"id":2591,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages\/1233\/revisions\/2591"}],"wp:attachment":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=1233"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}