{"id":1187,"date":"2025-09-17T20:11:50","date_gmt":"2025-09-17T18:11:50","guid":{"rendered":"https:\/\/neurokidbossa.rs\/?p=1187"},"modified":"2025-09-17T21:06:33","modified_gmt":"2025-09-17T19:06:33","slug":"rett-sindrom","status":"publish","type":"post","link":"https:\/\/neurokidbossa.rs\/en\/rett-sindrom\/","title":{"rendered":"Rett sindrom (RS)"},"content":{"rendered":"\n<p><\/p>\n\n\n\n<p><\/p>\n\n\n\n<p><strong>Rett sindrom<\/strong> je redak geneti\u010dki sindrom koji se karakteri\u0161e gubitkom motornih i govornih sposobnosti a koji rezultira ozbiljnom mentalnom i fizi\u010dkom deficijencijom. Za ispoljavanje klini\u010dkih simptoma odgovorna je mutacija na MECP2 genu, lociranom na dugom kraku polnog X hromozoma. Ova genetska mutacija se javlja sporadi\u010dno, de novo, i nije nasledna od roditelja. Smatra se da jedna od 10 000 devoj\u010dica mla\u0111ih od 12 godina, ima \u00a0Rett sindrom.<br><\/p>\n\n\n\n<p><br>Prvi klini\u010dki opis Rett sindroma dao je austrijski razvojni pedijatar, Anreas Rett 1966 (Rett, 1966) i u njegovu \u010dast sindrom sa klini\u010dkim karakteristikama koje je on prvi opisao, nosi njegovo ime.<\/p>\n\n\n\n<p><br>Spektar simptoma koji imaju devoj\u010dice sa Rett sindromom (retko se mutacija mo\u017ee na\u0107i i kod de\u010daka) je razli\u010dit i individualan za svaku osobu sa Rett sindromom, a simptomi se mogu menjati sa uzrastom. Pored neurolo\u0161kih i bihejvioralnih simptoma deca sa Rett sindromom mogu imati i druge medicinske probleme vezane za disanje, gastrointestinalni sistem, te ortopedske i kardiolo\u0161ke probleme.<\/p>\n\n\n\n<p><br><strong>Glavne karakteristike RS<\/strong> su regeresija pshomotornog razvoja gde se odoj\u010de uglavnom normalno razvija do 6, ili 9. meseca kada zapo\u010dinje regresija\u00a0 u smislu intenzivnih stereotipnih pokreta ruku i gubitka svrsishodnih pokreta ruku (dispraksija ruku) (Neul et al.2010). Drugi simptomi uklju\u010duju epilepti\u010dne napade, kognitivnu deterioraciju, skoliozu, problem hranjenja, zaostajanje u rastu, poreme\u0107aj spavanja, \u0161krgutanje zubima, hiperventilaciju, disfunkciju motornog i autonomnog sistema.<\/p>\n\n\n\n<p><br>Dva naj\u010de\u0161\u0107a simptoma su epilepti\u010dki napadi i problem disanja.<\/p>\n\n\n\n<p><br><strong>Epilepti\u010dni napadi<\/strong> bilo fokalni ili generalizovani, su retki do 3. godine \u017eivota a onda se javljaju sa ve\u0107om u\u010destalo\u0161\u0107u oko 8-10. godine (Percy et al 2024). Ve\u0107ina dece sa Rett sindromom ima epilepti\u010dne napade 60% (Glaze et al.2010), a po drugim podacima iz literature \u010dak u 80-94% (Steffenburg et al 2001). Uglavnom su napadi kontrolisani antiepilepti\u010dkom terapijom (ista pravila va\u017ee kao i pravila za ostale osobe obolele od epilepsije) \u00a0i samo su u 5-10% slu\u010dajeva napadi farmako rezistentni (ne reaguju na primenjenu medikamentoznu terapiju), kada se pribegava ketogenoj dijeti (KDT) ili vagalnoj nervnoj stimulaciji (VNS).<\/p>\n\n\n\n<p><br><strong>Poreme\u0107aj disanja<\/strong> bilo da se radi o breath holding atacima ili hiperventilaciji mogu ote\u017eavati svakodnevno \u017eivotno funkcionisanje, ometati hranjenje i fizioterapiju, kao i op\u0161tu negu. Najve\u0107e pote\u0161ko\u0107e su od 5-15 godine, posle 15. Godine imaju tendenciju opadanja, i uglavnom su vezane za hranjenje, fizioterapiju i komunikaciju sa roditeljima ili terapeutima.<\/p>\n\n\n\n<p><br><strong>Stereotipni pokreti ruku<\/strong> su prisutni skoro kod sve dece sa RS i uklju\u010duju tap\u0161anje, stiskanje ruku, pljeskanje, trljanje prstiju ili stavljanje ruke u usta.<\/p>\n\n\n\n<p><br>Rett sindrom prate i poreme\u0107aji drugih organa i Sistema kao sto su: gastro intestinalni trakt (problem hranjenja gastro-ezofagelani reflux, zatvor), poreme\u0107aj spavanja, skolioza (prisutna u cak 85% oboba sa RS), kontrakture, kardiolo\u0161ke smetnje (produ\u017een QT interval), poreme\u0107aj pona\u0161anja, anksioznost.<\/p>\n\n\n\n<p><br>Zbog kompleksnosti sindroma, neophodan je multidisciplinarni pristup sa uklju\u010divanjem razli\u010ditih subspecijalnosti kao sto su: de\u010dji neurolog\/epileptolog, de\u010diji gastroenterolog, ortoped, fizijatar, pulmolog, kardiolog i druge specijalnosti od zna\u010daja.<\/p>\n\n\n\n<p><br>Prose\u010dan \u017eivotni vek osoba sa Rett sindromom je 40-50 godina, a smrt nastupa usled kardio-respiratorne insuficijencije, kao posledice aspiracione pneumonije, malnutricije ili epilepti\u010dnih napada.<\/p>\n\n\n\n<p><br>Klini\u010dka ispitivanja sa specifi\u010dnom terapijom Glatiramer acetatom (Djuki\u0107 et al. 2016.) \u00a0i Trofinetide (Neuel et al 2023;Percy et al.2024) daju nadu za pobolj\u0161anje klini\u010dkih simptoma i bolji kvalitet zivota osoba sa Rett sindromom i nihovih porodica.<\/p>\n\n\n\n<p><br>Rett udru\u017eenje u Srbiji:<\/p>\n\n\n\n<figure class=\"wp-block-embed is-type-wp-embed is-provider-rett-syndrome-europe wp-block-embed-rett-syndrome-europe\"><div class=\"wp-block-embed__wrapper\">\n<blockquote class=\"wp-embedded-content\" data-secret=\"yU25NR9DjX\"><a href=\"https:\/\/www.rettsyndrome.eu\/member-associations\/serbia\/\">Serbia<\/a><\/blockquote><iframe class=\"wp-embedded-content\" sandbox=\"allow-scripts\" security=\"restricted\" style=\"position: absolute; visibility: hidden;\" title=\"&#8220;Serbia&#8221; &#8212; Rett Syndrome Europe\" src=\"https:\/\/www.rettsyndrome.eu\/member-associations\/serbia\/embed\/#?secret=dreTmDXijE#?secret=yU25NR9DjX\" data-secret=\"yU25NR9DjX\" width=\"500\" height=\"282\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\"><\/iframe>\n<\/div><\/figure>\n\n\n\n<p><br>Internacionalno Udru\u017eenje osoba sa Rett sindromom.<\/p>\n\n\n\n<figure class=\"wp-block-embed is-type-wp-embed is-provider-international-rett-syndrome-foundation wp-block-embed-international-rett-syndrome-foundation\"><div class=\"wp-block-embed__wrapper\">\n<blockquote class=\"wp-embedded-content\" data-secret=\"0FWyVNOmS0\"><a href=\"https:\/\/www.rettsyndrome.org\/about-irsf\/contact-us\/\">Contact Us<\/a><\/blockquote><iframe class=\"wp-embedded-content\" sandbox=\"allow-scripts\" security=\"restricted\" style=\"position: absolute; visibility: hidden;\" title=\"&#8220;Contact Us&#8221; &#8212; International Rett Syndrome Foundation\" src=\"https:\/\/www.rettsyndrome.org\/about-irsf\/contact-us\/embed\/#?secret=OnXHPI0hK9#?secret=0FWyVNOmS0\" data-secret=\"0FWyVNOmS0\" width=\"500\" height=\"282\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\"><\/iframe>\n<\/div><\/figure>\n\n\n\n<figure class=\"wp-block-embed\"><div class=\"wp-block-embed__wrapper\">\nhttps:\/\/reverserett.org\n<\/div><\/figure>\n\n\n\n<p>Literatura:<\/p>\n\n\n\n<p><br>Rett A. On a unusual brain atrophy syndrome in hyperammonemia in childhood. Wien Med. Wochenschr. 1966;116:723\u2013726.\u00a0<\/p>\n\n\n\n<p><br>Neul Jeffery., Kaufmann W.E., Glaze D.G., Christodoulou J., Clarke A.J., Bahi-Buisson N., Leonard H., Bailey M.E.S., Schanen N.C., Zappella M., et al. Rett syndrome: Revised diagnostic criteria and nomenclature. Ann. Neurol. 2010;68:944\u2013950. doi: 10.1002\/ana.22124.<\/p>\n\n\n\n<p><br>Percy AK, Ananth A, Neul JL. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/39251501\/\"><strong>Rett<\/strong>\u00a0<strong>Syndrome<\/strong>: The Emerging Landscape of\u00a0<strong>Treatment<\/strong>\u00a0Strategies.<\/a>CNS Drugs. 2024 Nov;38(11):851-867. doi: 10.1007\/s40263-024-01106-y. Epub 2024 Sep 9.PMID:\u00a039251501<\/p>\n\n\n\n<p><br>Steffenburg U, Hagberg G, Hagberg B. Epilepsy in a representative series of Rett syndrome. Acta Paediatr 2001;90:34\u201339.\u00a0[<a href=\"https:\/\/doi.org\/10.1080\/080352501750064842\" target=\"_blank\" rel=\"noreferrer noopener\">DOI<\/a>] [<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/11227330\/\">PubMed<\/a>] [<a href=\"https:\/\/scholar.google.com\/scholar_lookup?Steffenburg%20U,%20Hagberg%20G,%20Hagberg%20B.%20Epilepsy%20in%20a%20representative%20series%20of%20Rett%20syndrome.%20Acta%20Paediatr%202001;90:34%E2%80%9339.\" target=\"_blank\" rel=\"noreferrer noopener\">Google Scholar<\/a>]<\/p>\n\n\n\n<p><br><a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22Glaze%20DG%22%5BAuthor%5D\">D G Glaze<\/a>\u00a0,\u00a0<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22Percy%20AK%22%5BAuthor%5D\">A K Percy<\/a>\u00a0,<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22Skinner%20S%22%5BAuthor%5D\">S Skinner<\/a>\u00a0,\u00a0<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22Motil%20KJ%22%5BAuthor%5D\">K J Motil<\/a>\u00a0,\u00a0<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22Neul%20JL%22%5BAuthor%5D\">J L Neul<\/a>\u00a0,\u00a0<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22Barrish%20JO%22%5BAuthor%5D\">J O Barrish<\/a>\u00a0,\u00a0<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22Lane%20JB%22%5BAuthor%5D\">J B Lane<\/a>,\u00a0<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22Geerts%20SP%22%5BAuthor%5D\">S P Geerts<\/a>\u00a0,\u00a0<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22Annese%20F%22%5BAuthor%5D\">F Annese<\/a>\u00a0,\u00a0<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22Graham%20J%22%5BAuthor%5D\">J Graham<\/a>\u00a0,<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22McNair%20L%22%5BAuthor%5D\">L McNair<\/a>\u00a0,<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22Lee%20HS%22%5BAuthor%5D\">H -S Lee<\/a>.\u00a0<\/p>\n\n\n\n<p><br><strong>Epilepsy and the natural history of Rett syndrome<\/strong><\/p>\n\n\n\n<p><br>Neurology. 2010 Mar 16;74(11):909\u2013912. doi:\u00a0<a href=\"https:\/\/doi.org\/10.1212\/WNL.0b013e3181d6b852\" target=\"_blank\" rel=\"noreferrer noopener\">10.1212\/WNL.0b013e3181d6b852<\/a><\/p>\n\n\n\n<p><br>Percy AK, Neul JL, Benke TA, Berry-Kravis EM, Glaze DG, Marsh ED, Barrett AM, An D, Bishop KM, Youakim JM. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/39025065\/\">Trofinetide for the\u00a0<strong>treatment<\/strong>\u00a0of\u00a0<strong>Rett<\/strong>\u00a0<strong>syndrome<\/strong>: Long-term safety and efficacy results of the 32-month, open-label LILAC-2 study.<\/a><\/p>\n\n\n\n<p><br>Med. 2024 Oct 11;5(10):1275-1281.e2. doi: 10.1016\/j.medj.2024.06.007. Epub 2024 Jul 17.PMID:\u00a039025065<\/p>\n\n\n\n<p><br><a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/27363291\/\">Pharmacologic\u00a0<strong>Treatment<\/strong>\u00a0of\u00a0<strong>Rett<\/strong>\u00a0<strong>Syndrome<\/strong>\u00a0With Glatiramer Acetate.<\/a><\/p>\n\n\n\n<p><br>Djukic A, Holtzer R, Shinnar S, Muzumdar H, Rose SA, Mowrey W, Galanopoulou AS, Shinnar R, Jankowski JJ, Feldman JF, Pillai S, Mosh\u00e9 SL.Pediatr Neurol. 2016 Aug;61:51-7. doi: 10.1016\/j.pediatrneurol.2016.05.010. Epub 2016 May 27.PMID:\u00a027363291\u00a0Clinical Trial.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Rett sindrom je redak geneti\u010dki sindrom koji se karakteri\u0161e gubitkom motornih i govornih sposobnosti a koji rezultira ozbiljnom mentalnom i fizi\u010dkom deficijencijom. Za ispoljavanje klini\u010dkih simptoma odgovorna je mutacija na MECP2 genu, lociranom na dugom kraku polnog X hromozoma. Ova genetska mutacija se javlja sporadi\u010dno, de novo, i nije nasledna od roditelja. Smatra se da [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"set","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"footnotes":""},"categories":[1],"tags":[],"class_list":["post-1187","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Rett sindrom (RS) - Neuro Kid Bossa<\/title>\n<meta name=\"description\" content=\"Rett sindrom je redak geneti\u010dki sindrom koji se karakteri\u0161e gubitkom motornih i govornih sposobnosti a koji rezultira ozbiljnom mentalnom i fizi\u010dkom deficijencijom.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/neurokidbossa.rs\/en\/rett-sindrom\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Rett sindrom (RS) - Neuro Kid Bossa\" \/>\n<meta property=\"og:description\" content=\"Rett sindrom je redak geneti\u010dki sindrom koji se karakteri\u0161e gubitkom motornih i govornih sposobnosti a koji rezultira ozbiljnom mentalnom i fizi\u010dkom deficijencijom.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/neurokidbossa.rs\/en\/rett-sindrom\/\" \/>\n<meta property=\"og:site_name\" content=\"Neuro Kid Bossa\" \/>\n<meta property=\"article:published_time\" content=\"2025-09-17T18:11:50+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2025-09-17T19:06:33+00:00\" \/>\n<meta name=\"author\" content=\"NeuroKidBossa\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"NeuroKidBossa\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"5 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/neurokidbossa.rs\\\/rett-sindrom\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/neurokidbossa.rs\\\/rett-sindrom\\\/\"},\"author\":{\"name\":\"NeuroKidBossa\",\"@id\":\"https:\\\/\\\/neurokidbossa.rs\\\/#\\\/schema\\\/person\\\/327dde3c5b320395051e440febe9eb83\"},\"headline\":\"Rett sindrom (RS)\",\"datePublished\":\"2025-09-17T18:11:50+00:00\",\"dateModified\":\"2025-09-17T19:06:33+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/neurokidbossa.rs\\\/rett-sindrom\\\/\"},\"wordCount\":836,\"commentCount\":0,\"publisher\":{\"@id\":\"https:\\\/\\\/neurokidbossa.rs\\\/#organization\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"CommentAction\",\"name\":\"Comment\",\"target\":[\"https:\\\/\\\/neurokidbossa.rs\\\/rett-sindrom\\\/#respond\"]}]},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/neurokidbossa.rs\\\/rett-sindrom\\\/\",\"url\":\"https:\\\/\\\/neurokidbossa.rs\\\/rett-sindrom\\\/\",\"name\":\"Rett sindrom (RS) - Neuro Kid Bossa\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/neurokidbossa.rs\\\/#website\"},\"datePublished\":\"2025-09-17T18:11:50+00:00\",\"dateModified\":\"2025-09-17T19:06:33+00:00\",\"description\":\"Rett sindrom je redak geneti\u010dki sindrom koji se karakteri\u0161e gubitkom motornih i govornih sposobnosti a koji rezultira ozbiljnom mentalnom i fizi\u010dkom deficijencijom.\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/neurokidbossa.rs\\\/rett-sindrom\\\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/neurokidbossa.rs\\\/rett-sindrom\\\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/neurokidbossa.rs\\\/rett-sindrom\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\\\/\\\/neurokidbossa.rs\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Rett sindrom (RS)\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/neurokidbossa.rs\\\/#website\",\"url\":\"https:\\\/\\\/neurokidbossa.rs\\\/\",\"name\":\"Neuro Kid Bossa\",\"description\":\"De\u010dija neurologija i EEG dijagnostika\",\"publisher\":{\"@id\":\"https:\\\/\\\/neurokidbossa.rs\\\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/neurokidbossa.rs\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Organization\",\"@id\":\"https:\\\/\\\/neurokidbossa.rs\\\/#organization\",\"name\":\"Neuro Kid Bossa\",\"url\":\"https:\\\/\\\/neurokidbossa.rs\\\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\\\/\\\/neurokidbossa.rs\\\/#\\\/schema\\\/logo\\\/image\\\/\",\"url\":\"https:\\\/\\\/neurokidbossa.rs\\\/wp-content\\\/uploads\\\/2023\\\/01\\\/cropped-Neuro-Kid-Bossa-b-1.png\",\"contentUrl\":\"https:\\\/\\\/neurokidbossa.rs\\\/wp-content\\\/uploads\\\/2023\\\/01\\\/cropped-Neuro-Kid-Bossa-b-1.png\",\"width\":500,\"height\":459,\"caption\":\"Neuro Kid Bossa\"},\"image\":{\"@id\":\"https:\\\/\\\/neurokidbossa.rs\\\/#\\\/schema\\\/logo\\\/image\\\/\"}},{\"@type\":\"Person\",\"@id\":\"https:\\\/\\\/neurokidbossa.rs\\\/#\\\/schema\\\/person\\\/327dde3c5b320395051e440febe9eb83\",\"name\":\"NeuroKidBossa\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/dbe86cfc9bd372c9ac2ab8ca755864f1b8f8c4049269cb5e271d528b9a3f34a4?s=96&d=mm&r=g\",\"url\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/dbe86cfc9bd372c9ac2ab8ca755864f1b8f8c4049269cb5e271d528b9a3f34a4?s=96&d=mm&r=g\",\"contentUrl\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/dbe86cfc9bd372c9ac2ab8ca755864f1b8f8c4049269cb5e271d528b9a3f34a4?s=96&d=mm&r=g\",\"caption\":\"NeuroKidBossa\"},\"sameAs\":[\"https:\\\/\\\/neurokidbossa.rs\"],\"url\":\"https:\\\/\\\/neurokidbossa.rs\\\/en\\\/author\\\/j0vko\\\/\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Rett sindrom (RS) - Neuro Kid Bossa","description":"Rett sindrom je redak geneti\u010dki sindrom koji se karakteri\u0161e gubitkom motornih i govornih sposobnosti a koji rezultira ozbiljnom mentalnom i fizi\u010dkom deficijencijom.","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/neurokidbossa.rs\/en\/rett-sindrom\/","og_locale":"en_US","og_type":"article","og_title":"Rett sindrom (RS) - Neuro Kid Bossa","og_description":"Rett sindrom je redak geneti\u010dki sindrom koji se karakteri\u0161e gubitkom motornih i govornih sposobnosti a koji rezultira ozbiljnom mentalnom i fizi\u010dkom deficijencijom.","og_url":"https:\/\/neurokidbossa.rs\/en\/rett-sindrom\/","og_site_name":"Neuro Kid Bossa","article_published_time":"2025-09-17T18:11:50+00:00","article_modified_time":"2025-09-17T19:06:33+00:00","author":"NeuroKidBossa","twitter_card":"summary_large_image","twitter_misc":{"Written by":"NeuroKidBossa","Est. reading time":"5 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/neurokidbossa.rs\/rett-sindrom\/#article","isPartOf":{"@id":"https:\/\/neurokidbossa.rs\/rett-sindrom\/"},"author":{"name":"NeuroKidBossa","@id":"https:\/\/neurokidbossa.rs\/#\/schema\/person\/327dde3c5b320395051e440febe9eb83"},"headline":"Rett sindrom (RS)","datePublished":"2025-09-17T18:11:50+00:00","dateModified":"2025-09-17T19:06:33+00:00","mainEntityOfPage":{"@id":"https:\/\/neurokidbossa.rs\/rett-sindrom\/"},"wordCount":836,"commentCount":0,"publisher":{"@id":"https:\/\/neurokidbossa.rs\/#organization"},"inLanguage":"en-US","potentialAction":[{"@type":"CommentAction","name":"Comment","target":["https:\/\/neurokidbossa.rs\/rett-sindrom\/#respond"]}]},{"@type":"WebPage","@id":"https:\/\/neurokidbossa.rs\/rett-sindrom\/","url":"https:\/\/neurokidbossa.rs\/rett-sindrom\/","name":"Rett sindrom (RS) - Neuro Kid Bossa","isPartOf":{"@id":"https:\/\/neurokidbossa.rs\/#website"},"datePublished":"2025-09-17T18:11:50+00:00","dateModified":"2025-09-17T19:06:33+00:00","description":"Rett sindrom je redak geneti\u010dki sindrom koji se karakteri\u0161e gubitkom motornih i govornih sposobnosti a koji rezultira ozbiljnom mentalnom i fizi\u010dkom deficijencijom.","breadcrumb":{"@id":"https:\/\/neurokidbossa.rs\/rett-sindrom\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/neurokidbossa.rs\/rett-sindrom\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/neurokidbossa.rs\/rett-sindrom\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/neurokidbossa.rs\/"},{"@type":"ListItem","position":2,"name":"Rett sindrom (RS)"}]},{"@type":"WebSite","@id":"https:\/\/neurokidbossa.rs\/#website","url":"https:\/\/neurokidbossa.rs\/","name":"Neuro Kid Bossa","description":"De\u010dija neurologija i EEG dijagnostika","publisher":{"@id":"https:\/\/neurokidbossa.rs\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/neurokidbossa.rs\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"},{"@type":"Organization","@id":"https:\/\/neurokidbossa.rs\/#organization","name":"Neuro Kid Bossa","url":"https:\/\/neurokidbossa.rs\/","logo":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/neurokidbossa.rs\/#\/schema\/logo\/image\/","url":"https:\/\/neurokidbossa.rs\/wp-content\/uploads\/2023\/01\/cropped-Neuro-Kid-Bossa-b-1.png","contentUrl":"https:\/\/neurokidbossa.rs\/wp-content\/uploads\/2023\/01\/cropped-Neuro-Kid-Bossa-b-1.png","width":500,"height":459,"caption":"Neuro Kid Bossa"},"image":{"@id":"https:\/\/neurokidbossa.rs\/#\/schema\/logo\/image\/"}},{"@type":"Person","@id":"https:\/\/neurokidbossa.rs\/#\/schema\/person\/327dde3c5b320395051e440febe9eb83","name":"NeuroKidBossa","image":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/secure.gravatar.com\/avatar\/dbe86cfc9bd372c9ac2ab8ca755864f1b8f8c4049269cb5e271d528b9a3f34a4?s=96&d=mm&r=g","url":"https:\/\/secure.gravatar.com\/avatar\/dbe86cfc9bd372c9ac2ab8ca755864f1b8f8c4049269cb5e271d528b9a3f34a4?s=96&d=mm&r=g","contentUrl":"https:\/\/secure.gravatar.com\/avatar\/dbe86cfc9bd372c9ac2ab8ca755864f1b8f8c4049269cb5e271d528b9a3f34a4?s=96&d=mm&r=g","caption":"NeuroKidBossa"},"sameAs":["https:\/\/neurokidbossa.rs"],"url":"https:\/\/neurokidbossa.rs\/en\/author\/j0vko\/"}]}},"_links":{"self":[{"href":"https:\/\/neurokidbossa.rs\/en\/wp-json\/wp\/v2\/posts\/1187","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/neurokidbossa.rs\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/neurokidbossa.rs\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/neurokidbossa.rs\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/neurokidbossa.rs\/en\/wp-json\/wp\/v2\/comments?post=1187"}],"version-history":[{"count":5,"href":"https:\/\/neurokidbossa.rs\/en\/wp-json\/wp\/v2\/posts\/1187\/revisions"}],"predecessor-version":[{"id":1195,"href":"https:\/\/neurokidbossa.rs\/en\/wp-json\/wp\/v2\/posts\/1187\/revisions\/1195"}],"wp:attachment":[{"href":"https:\/\/neurokidbossa.rs\/en\/wp-json\/wp\/v2\/media?parent=1187"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/neurokidbossa.rs\/en\/wp-json\/wp\/v2\/categories?post=1187"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/neurokidbossa.rs\/en\/wp-json\/wp\/v2\/tags?post=1187"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}