{"id":71625,"date":"2017-11-09T13:48:56","date_gmt":"2017-11-09T13:48:56","guid":{"rendered":"http:\/\/humanitasnet-new.local\/malattie\/stiklerov-sindrom\/"},"modified":"2025-01-13T03:00:56","modified_gmt":"2025-01-13T03:00:56","slug":"stiklerov-sindrom","status":"publish","type":"disease","link":"https:\/\/humanitas-net.humweb.webiz.team\/sr\/diseases\/stiklerov-sindrom\/","title":{"rendered":"Stiklerov sindrom"},"content":{"rendered":"<p>Stiklerov sindrom je genetsko stanje koje se stalno razvija, a koje se prenosi sa roditelja na dete. Ono je obi\u010dno dijagnostifikovano u ranom detinjstvu ili malo kasnije tokom detinjstva. Siklerov sindrom karakteri\u0161u abnormalnosti oka, izgleda lica (nerazvijene kosti srednjeg dela lica), rscepljeno nepce, manja donja vilica i prroblemi sa zglobovima.<\/p>\n<p>Ovo stanje uti\u010de na vezivno tkivo u telu (kolagen). Geni koji kontroli\u0161u sintezu kolagena i koji mogu da izazovu ovaj sindrom su:<\/p>\n<p>COL2A1- u 75% slu\u010dajeva i zato je poznat kao Stiklerov sindrom prvog tipa<\/p>\n<p>COL11A1- mo\u017ee uticati na zglobove, \u010dulo sluha, vida, poznat jo\u0161 i kao Stiklerov sindrom drugog tipa<\/p>\n<p>COL11A2- uti\u010de samo na zglobove i \u010dulo sluha, poznat kao Otospondilomegaepifizealna displasija<\/p>\n<p>Postoje jo\u0161 dva gena COL9A1 i COL9A2 koji se odnose na tre\u0107i i \u010detvrti tip Stiklerovog sindroma.<\/p>\n<p>Ovaj sindrom mo\u017ee da pogodi oba pola.<\/p>\n<p>&nbsp;<\/p>\n<h2 id=\"simptomi\">Simptomi<\/h2>\n<p>Simptomi stiklerovog sindroma su:<\/p>\n<p>Problemi sa o\u010dima, kao \u0161to su kratkovidost, glaukom, katarakte, odvajanje mre\u017enja\u010de<\/p>\n<p>Problemi sa sluhom- uglavnom se odnose na visoke frekvencije<\/p>\n<p>Nenormalnosti u kostima i zglobovima- ovi pacijenti koji imaju savitljive zglobove mogu da dobiju skoliozu<\/p>\n<p>Uko\u010deni zglobovi<\/p>\n<p>Rana bolest zglobova koja dovodi do osteoartritisa kasnije u \u017eivotu<\/p>\n<p>Rascepljeno nepce, sluzavo ili nepce sa visokim lukom<\/p>\n<p>Manja donja vilica<\/p>\n<p>Ravno lice, mali nos, sa malim ili bez ikakve nosne kosti<\/p>\n<p>Prolaps mitralnog zaliska<\/p>\n<p>&nbsp;<\/p>\n<h2 id=\"uzroci\">Uzroci<\/h2>\n<p>Uzrok Stiklerovog sindroma je mutacija nekih gena kolagena, koji su nasle\u0111eni od roditelja, naj\u010de\u0161\u0107e geni kolagena koji stvaraju\u00a0 hrskavicu zglobova i \u017eelatinasti deo oka.<\/p>\n<p>Veoma su retki slu\u010dajevi kada je do\u0161lo do ove bolesti a da nije prene\u0161ena sa roditelja koji je ve\u0107 imao.<\/p>\n<p>&nbsp;<\/p>\n<h2 id=\"komplikacije\">Komplikacije<\/h2>\n<p>Komplikacije kod Stiklerovog sindroma su:<\/p>\n<p>Te\u0161ko\u0107e u ishrani ako je dete ro\u0111eno sa pocepanihm nepcem<\/p>\n<p>Problemi sa zubima usled male vilice<\/p>\n<p>Infekcija uha<\/p>\n<p>Slepilo, u slu\u010daju glaukoma ili katarakte<\/p>\n<p>Problemi sa srcem<\/p>\n","protected":false},"featured_media":0,"template":"","class_list":["post-71625","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>Stiklerov sindrom - 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=\"sr_RS\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Stiklerov sindrom - Humanitas.net\" \/>\n<meta property=\"og:description\" content=\"Stiklerov sindrom je genetsko stanje koje se stalno razvija, a koje se prenosi sa roditelja na dete. 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