{"id":260500,"date":"2026-08-25T12:49:21","date_gmt":"2026-08-25T12:49:21","guid":{"rendered":"https:\/\/www.europesays.com\/ee\/260500\/"},"modified":"2026-08-25T12:49:21","modified_gmt":"2026-08-25T12:49:21","slug":"aitame-koos-%e2%9f%a9-17-aastase-eesti-neiu-elupaastev-ravi-maksab-300-000-eurot","status":"publish","type":"post","link":"https:\/\/www.europesays.com\/ee\/260500\/","title":{"rendered":"AITAME KOOS \u27e9 17-aastase Eesti neiu elup\u00e4\u00e4stev ravi maksab 300 000 eurot"},"content":{"rendered":"<p>Viktorial on diagnoositud \u00fcliharuldane rasvade ladestumise haigus LAL-D ehk l\u00fcsosomaalhappeline ladestushaigus, mida p\u00f5hjustab LIPA geeni mutatsioon. See on harvikhaigus, mille esinemisagedus on hinnanguliselt vaid 2,5 haigusjuhtu k\u00fcmne tuhande s\u00fcnni kohta ja Eestis on sama haigus teadaolevalt veel vaid \u00fchel 21-aastasel naisel.<\/p>\n<p>Haiguse t\u00f5ttu ei suuda organism teatud rasvu normaalselt lagundada. Rasvad hakkavad kogunema maksarakkudesse ja veresoonte seintesse ning p\u00f5hjustavad aasta-aastalt \u00fcha suuremat kahjustust.<\/p>\n<p>Vaikne, aga ohtlik h\u00e4vitust\u00f6\u00f6<\/p>\n<p><img decoding=\"async\" class=\"figure__image\" onclick=\"triggerEvent('articleImageClick', { id: 17876704, focus: 'single-image', focusIndex: '17876704' })\" onkeydown=\"if (event.key === 'Enter') {&#10;        triggerEvent('articleImageClick', { id: 17876704, focus: 'single-image', focusIndex: '17876704' })&#10;        }\" role=\"button\" tabindex=\"0\" data-focus-from=\"single-image\" data-focus-index=\"17876704\" src=\"https:\/\/www.europesays.com\/ee\/wp-content\/uploads\/2026\/08\/17876704t1h91d2.jpg\"  onload=\"this.parentElement.classList.remove('figure__image-loading')\" alt=\"Viktoria armastab v\u00e4ga kunsti ja unistab tulevikus arhitektuuri v\u00f5i ehitusinseneeria \u00f5ppimisest.\"\/>Viktoria armastab v\u00e4ga kunsti ja unistab tulevikus arhitektuuri v\u00f5i ehitusinseneeria \u00f5ppimisest. Foto: Erakogu<\/p>\n<p>Olukorra tegi keeruliseks see, et aastaid ei teadnud keegi, mis t\u00fcdruku organismis tegelikult toimub. Esimesed m\u00e4rgid haigusest ilmnesid juba lapseeas, mil Viktoria silmad muutusid aeg-ajalt kollaseks ning vereanal\u00fc\u00fcsid n\u00e4itasid k\u00f5rvalekaldeid maksatalitluses.<\/p>\n<p>11-aastaselt sattus t\u00fcdruk tugeva rindkerevalu t\u00f5ttu haiglasse ja 2020. aastal tehti talle esimene maksabiopsia. See uuring ei toonud veel l\u00f5plikku selgust. Alles 2024. aastal, mil geenitehnoloogia oli t\u00e4iustunud, tehti kordusuuringuid ja uus maksabiopsia, selgus t\u00e4pne diagnoos. Uuringust n\u00e4htus \u00fchtlasi, et maksakahjustus oli ajaga s\u00fcvenenud.<\/p>\n<p>Viktoria raviarsti, Tallinna Lastehaigla arsti dr Mari-Liis Kummi s\u00f5nul v\u00f5ib haigus viia maksa rasvumise, fibroosi ja l\u00f5puks tsirroosini, samuti kaasneb varajase ateroskleroosi risk. Ilma ravita vajaks neiu peatselt maksasiirdamist. \u00abSee on haigus, mis v\u00f5ib alguses j\u00e4\u00e4da peaaegu m\u00e4rkamatuks,\u00bb selgitab dr Kumm. \u00abV\u00e4liselt v\u00f5ib laps tunduda \u00fcsna terve, kuid samal ajal kahjustab haigus vaikselt maksa.\u00bb<\/p>\n<p>Aastaid kestnud teadmatus ja kurb t\u00f5de<\/p>\n<p>\u00abSee kohtumine arstiga oli v\u00e4ga kurb,\u00bb meenutab Viktoria hetke, mil diagnoos selgus. \u00abSiis \u00f6eldi esimest korda, et v\u00f5ib-olla l\u00e4heb tulevikus vaja maksasiirdamist.\u00bb<\/p>\n","protected":false},"excerpt":{"rendered":"Viktorial on diagnoositud \u00fcliharuldane rasvade ladestumise haigus LAL-D ehk l\u00fcsosomaalhappeline ladestushaigus, mida p\u00f5hjustab LIPA geeni mutatsioon. See on&hellip;\n","protected":false},"author":2,"featured_media":260501,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":"","_share_on_mastodon":"0"},"categories":[12],"tags":[9937,26,27,37,33,35,101201,34,36,31,32,101203,4022,21,101200,28,29,101202,101199,51201,36323,92076,19,25,4018,23,24,22,20,30],"class_list":["post-260500","post","type-post","status-publish","format-standard","has-post-thumbnail","category-eesti","tag-annetamine","tag-breaking-news","tag-breakingnews","tag-ee","tag-eesti","tag-eesti-keel","tag-ensuumasendusravi","tag-estonia","tag-estonian","tag-featured-news","tag-featurednews","tag-geneetiline-haigus","tag-harvikhaigus","tag-headlines","tag-lal-d","tag-latest-news","tag-latestnews","tag-lipa-geen","tag-lusosomaalhappeline-ladestushaigus","tag-maksahaigus","tag-maksakahjustus","tag-maksasiirdamine","tag-news","tag-populaarseimad-lood","tag-tallinna-lastehaigla-toetusfond","tag-top-stories","tag-topstories","tag-uldised-uudised","tag-uudised","tag-viimased-uudised"],"share_on_mastodon":{"url":"","error":"Validation failed: Text character limit of 500 exceeded"},"_links":{"self":[{"href":"https:\/\/www.europesays.com\/ee\/wp-json\/wp\/v2\/posts\/260500","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.europesays.com\/ee\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.europesays.com\/ee\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ee\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ee\/wp-json\/wp\/v2\/comments?post=260500"}],"version-history":[{"count":0,"href":"https:\/\/www.europesays.com\/ee\/wp-json\/wp\/v2\/posts\/260500\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ee\/wp-json\/wp\/v2\/media\/260501"}],"wp:attachment":[{"href":"https:\/\/www.europesays.com\/ee\/wp-json\/wp\/v2\/media?parent=260500"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.europesays.com\/ee\/wp-json\/wp\/v2\/categories?post=260500"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.europesays.com\/ee\/wp-json\/wp\/v2\/tags?post=260500"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}