{"id":73026,"date":"2020-10-28T14:00:32","date_gmt":"2020-10-28T14:00:32","guid":{"rendered":"http:\/\/humanitasnet-new.local\/malattie\/sindrom-trojnega-x\/"},"modified":"2025-01-13T03:20:42","modified_gmt":"2025-01-13T03:20:42","slug":"sindrom-trojnega-x","status":"publish","type":"disease","link":"https:\/\/humanitas-net.humweb.webiz.team\/sl\/diseases\/sindrom-trojnega-x\/","title":{"rendered":"Sindrom trojnega X"},"content":{"rendered":"<p>Za sindrom trojnega X (trisomijo) je zna\u010dilna prisotnost dodatnega X kromosoma v vsaki celici \u017eenske. \u017denske imajo obi\u010dajno dva X kromosoma, po enega od vsakega star\u0161a. Pri sindromu trojnega X ima \u017eenska tri kromosome X in od tod izvira ime motnje. \u010ceprav so \u017eenske s tem stanjem lahko vi\u0161je od povpre\u010dnih, ta kromosomska sprememba obi\u010dajno ne povzro\u010da nobenih nenavadnih fizi\u010dnih lastnosti.<\/p>\n<p>Ve\u010dina \u017eensk s sindromom trojnega X ima normalen spolni razvoj in lahko spo\u010dne otroke. Vendar pa je to stanje povezano s pove\u010danim tveganjem za u\u010dne te\u017eave in z zamudo pri razvoju govornih in jezikovnih spretnosti. Mo\u017eni so tudi zapozneli razvoj motori\u010dnih sposobnosti, \u0161ibek mi\u0161i\u010dni tonus ter vedenjske in \u010dustvene te\u017eave, vendar se te zna\u010dilnosti med prizadetimi dekleti in \u017eenskami zelo razlikujejo.<\/p>\n<h2 id=\"simptomi\">Simptomi<\/h2>\n<p>Simptomi trojnega sindroma X so lahko:<\/p>\n<ul>\n<li>Zapoznel razvoj govornih in jezikovnih ve\u0161\u010din<\/li>\n<li>Visoka rast<\/li>\n<li>Navpi\u010dne ko\u017ene gube, ki lahko prekrivajo notranje koti\u010dke o\u010di<\/li>\n<li>\u0160ibek mi\u0161i\u010dni tonus<\/li>\n<li>Ukrivljeni ro\u017enati prsti<\/li>\n<li>Vedenje in te\u017eave z du\u0161evnim zdravjem<\/li>\n<li>Prezgodnja odpoved jaj\u010dnikov ali nepravilnosti jaj\u010dnikov<\/li>\n<li>Zaprtje ali bole\u010dine v trebuhu<\/li>\n<\/ul>\n<h2 id=\"vzroki\">Vzroki<\/h2>\n<p>Obi\u010dajno ima 46 kromosomov, ki se pojavljajo v 22 parih, plus dva spolna kromosoma, en materinski in en o\u010detovski. Ti kromosomi vsebujejo gene, ki vsebujejo navodila, ki dolo\u010dajo vse o \u010dloveku.<\/p>\n<p>Par kromosomov, ki dolo\u010da spol, vklju\u010duje en spolni kromosom matere in drugega od o\u010deta. Mati lahko daje samo X kromosom X, o\u010de pa prenese X ali Y kromosom. \u010ce od o\u010deta prejmete X kromosom X, vas par XX genetsko naredi \u017eensko. \u010ce od o\u010deta prejmete Y kromosom Y, potem par XY pomeni, da ste genetsko mo\u0161ki.<\/p>\n<p>\u017denske s sindromom trojnega X imajo tretji X kromosom. Ta pogoj je genetski, vendar se obi\u010dajno ne podeduje. Obi\u010dajno se zgodi, da se materina jaj\u010dna celica ali o\u010detova semen\u010dica nista pravilno oblikovala, kar ima za posledico dodaten X kromosom.<\/p>\n<p>V primeru nepravilno oblikovane jaj\u010dne celice se dodatni kromosom lahko pojavi \u0161ele zgodaj v razvoju zarodka. V tem primeru ima \u017eenska mozai\u010dno obliko sindroma trojnega X. V primeru mozai\u010dne oblike imajo le nekatere celice telesa tretji X kromosom. Te \u017eenske imajo lahko manj hude simptome.<\/p>\n<h2 id=\"dejavniki-tveganja\">Dejavniki tveganja<\/h2>\n<p>Geni so osnovni del celotnega obstoja \u010dloveka. Odlo\u010dajo o vedenju v okolju, kako \u010dlovek \u017eivi in \u200b\u200bkak\u0161en je \u010dlovek. Tovrstna bolezen se zgodi zelo redko in se zgodi le pri \u017eenskah. Drugo ime za ta sindrom bolezni je 47, XXX sindrom, ker ima oseba dodaten X kromosom, 47 namesto 46 kromosomov.<\/p>\n<h2 id=\"zapleti\">Zapleti<\/h2>\n<p>Zamude pri razvoju ali u\u010dne ovire so zapleti, ki lahko nastanejo zaradi sindroma trojnega X, ki lahko privede do drugih vpra\u0161anj, vklju\u010dujo\u010d te\u017eave v karieri ter stres in socialno izolacijo.<\/p>\n<p>Drugi zapleti, ki se lahko pojavijo, \u010deprav redko, so:<\/p>\n<ul>\n<li>Epilepti\u010dni napadi.<\/li>\n<li>Prezgodnja odpoved jaj\u010dnikov ali nepravilnosti jaj\u010dnikov.<\/li>\n<li>Nenormalnosti ledvic.<\/li>\n<\/ul>\n<h2 id=\"preprecevanje\">Prepre\u010devanje<\/h2>\n<p>Spremembe kromosoma, ki povzro\u010di sindrom trojnega X, ni mogo\u010de popraviti, zato se sindroma samega ne zdravi in \u200b\u200bga ni mogo\u010de prepre\u010diti. Vendar pa je glede na ozdravljivo naravo ve\u010dine simptomov in pogostost pojava, da simptomov sploh ni, povsem mogo\u010de, da s tem sindromom vodimo in \u017eivimo polno in normalno \u017eivljenje.<\/p>\n","protected":false},"featured_media":0,"template":"","class_list":["post-73026","disease","type-disease","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.3 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Sindrom trojnega X - Humanitas.net<\/title>\n<meta name=\"robots\" content=\"noindex, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<meta property=\"og:locale\" content=\"sl_SI\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Sindrom trojnega X - Humanitas.net\" \/>\n<meta property=\"og:description\" content=\"Za sindrom trojnega X (trisomijo) je zna\u010dilna prisotnost dodatnega X kromosoma v vsaki celici \u017eenske. \u017denske imajo obi\u010dajno dva X kromosoma, po enega od vsakega star\u0161a. 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