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SMA Hastalığı Nedir? SMA Belirtileri...","preview":{"posterSrc":"//avatars.mds.yandex.net/get-vthumb/3192075/08f2f1b297b5b4874c362b43a38e99b5/564x318_1"},"target":"_self","position":"1","reqid":"1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL","summary":{"fullTextUrl":"/int_search_summary?data=http%3A%2F%2Fwww.youtube.com%2Fwatch%3Fv%3DnNAhZv7u0CM","linkTemplate":"/video/preview/5624346292161898252?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=%%timestamp%%&ask_summarization=1"},"isAdultDoc":false,"relatedParams":{"text":"SMA Hastalığı Nedir SMA Belirtileri, Nedenleri ve Tedavisi","related_orig_text":"sma","related_porno":false,"related_less_3m_off":true,"client":"d2d","no_cnt":1,"related_src":"serp","related":"{\"porno\":false,\"vfp\":1,\"orig_text\":\"sma\",\"url\":\"http:\\/\\/www.youtube.com\\/watch?v=nNAhZv7u0CM\",\"src\":\"serp\",\"rvb\":\"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_P0O_gIAA_X7CQYJ_AID-Q0B-f7-APICEQX9Af8A9_kA9wEAAADqA_oA9wAAAP_u9Qj9_gAAEez7_QEAAAAG-v3_-gAAAPEB_fX_AQAABwv4-wMAAAAWBf4GAAAAAPwMB_8CAAAADfT_AgEAAAAI7Av5AAAAACAALdOk2js4E0AJSE5QAipzEAAaYAIAAE0R_f7XBRjuEzkREOPmAjPtyev_ICkAzVviqwUwzusROQApJhrwrAAAABX49AvyAOFvvhX0-vxIEY73_v3vfyPtIdMjI87e-8o3AtIH-ytgIgDjCrXdOOuaIvUZ_CAALXsEHTs4E0AJSG9QAiqvBhAMGqAGAABAQQAAAEAAAEBBAADAQQAAmMEAAEBAAAAgQgAACMIAAABAAABAwAAA2EEAANhBAABIwgAAcEEAAFhCAACQwQAAIMEAADDCAAAAwQAAmMIAAMBAAABAwgAAAEAAAGBCAADWQgAAuEEAAIA_AACwwgAAaEIAABjCAACoQQAABEIAABTCAAAQwQAAoMAAAEBAAAC4QQAA4EAAAKBAAAAwwQAAQEAAAKDAAAAMwgAAPEIAADRCAAAIwgAApMIAAGDCAADQQQAA4EEAAAjCAACIwQAA2MEAAIDAAACYQQAA-MEAAJLCAAAIQgAASMIAADRCAACgwQAAAAAAAFjCAAD4wQAA8MEAAOBAAABAQgAAyMEAAHBBAAA8QgAAiMEAAIJCAADowQAAiEIAAEDAAADAwQAAuEEAACDBAADYwQAAQEAAAEBBAADAwAAAYMEAACBBAADYQQAASEIAADDCAADIwQAAGEIAAFBBAABAwAAAZEIAAIxCAADAQQAA-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-AABMPgAAhr4AACy-AABsPgAADL4AANi9AAATvwAAQDwAABQ-AAC4PQAAuL0AAEQ-AADYvQAADD4AAGy-AACIvQAAiD0AAJY-AADWPgAAfz8AACS-AACYPQAArr4AABA9AABQPQAA4LwAAFw-AACOvgAAyD0AACQ-AAAcPgAADD4AAJg9AACePgAALL4AABS-AADIvQAATL4AAKi9AABMPgAA6D0AAIi9AACSvgAAjj4AAAS-AACovQAARL4AAHS-AABkvgAAQDwAAJ4-AAA0PgAAqD0AAIA7AABwPQAAyj4AAFC9AACOPgAApj4AALg9AAA8vgAANL4AAK6-IAA4E0AJSHxQASqPAhABGoACAADIPQAACz8AACS-AABlvwAAD78AACQ-AABPPwAAED0AACw-AACiPgAAgLsAANa-AAB8vgAAor4AAKg9AACIPQAAcD0AAAs_AAAUvgAAoj4AAAy-AAC2vgAAfL4AAAQ-AAAUvgAAtj4AAES-AAAEPgAAXL4AAKq-AAAEvgAAyL0AADA9AAD4vQAAor4AAMg9AABcPgAA-L0AANi9AACivgAAqD0AAJ4-AADYPQAAgDsAAKA8AACePgAAf78AAOi9AADYvQAAoDwAAFA9AACCPgAAVD4AADC9AABUvgAADD4AANi9AAD4PQAAbD4AAOi9AABsPgAAoLwAABy-AACSPiAAOBNACUh8UAEwCTgBSgBgAGgA\"}","related_url":"http://www.youtube.com/watch?v=nNAhZv7u0CM","parent-reqid":"1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL","related_vfp":1,"relatedVideo":"yes"},"cwidth":1280,"cheight":720,"cratio":1.77777,"dups":["5624346292161898252"],"episode":0,"season":0,"isEmbedOnly":false,"greenHost":"YouTube","hasTranslation":true,"contentTypeId":null,"censored":false,"censoredShock":false,"isShockDoc":false},"11379171903082740736":{"videoId":"11379171903082740736","docid":"34-8-16-Z149CBA5B13F4E74F","description":"Türkiye'de son birkaç aydır daha çok kişi tarafından duyulsa da, SMA hastalığı olan çocukların aileleri yıllardır mücadele veriyor, tedavi masrafı için tek tek kampanya başlatıyorlar. Son olarak...","preview":{"posterSrc":"//avatars.mds.yandex.net/get-vthumb/2444666/4929019704f7920e40d709bde75b769b/564x318_1","videoSrc":"https://video-preview.s3.yandex.net/EDjQdgEAAAA.mp4","videoType":"video/mp4"},"target":"_self","position":"2","reqid":"1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL","summary":{"fullTextUrl":"/int_search_summary?data=http%3A%2F%2Fwww.youtube.com%2Fwatch%3Fv%3D3BMkgw5PoG0","linkTemplate":"/video/preview/11379171903082740736?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=%%timestamp%%&ask_summarization=1"},"isAdultDoc":false,"relatedParams":{"text":"SMA Hastaliği Nedir ? 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Today, we'll answer the question: What is SMA? SMA, or Spinal Muscular Atrophy, is a genetic disorder in which nerve cells in the spinal cord die prematurely, leading...","preview":{"posterSrc":"//avatars.mds.yandex.net/get-vthumb/3918131/7b029161ab260a7f8c639b8ddc973be3/564x318_1","videoSrc":"https://video-preview.s3.yandex.net/eR05LQIAAAA.mp4","videoType":"video/mp4"},"target":"_self","position":"6","reqid":"1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL","summary":{"fullTextUrl":"/int_search_summary?data=http%3A%2F%2Fwww.youtube.com%2Fwatch%3Fv%3DaZR8CIAzwuc","linkTemplate":"/video/preview/3906794714705230341?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=%%timestamp%%&ask_summarization=1"},"isAdultDoc":false,"relatedParams":{"text":"What is 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30 ile 50 bin arasında SMA hastası bulunmaktadır. Bu sayıya göre ortalama 50 kişiden biri SMA taşıyıcısıdır. Spinal Musküler Atrofi’nin kısaltılması olan SMA, bireyin merkezi ve...","preview":{"posterSrc":"//avatars.mds.yandex.net/get-vthumb/2713901/77298612c6a82bb2b1b2fdb7d5534bc9/564x318_1","videoSrc":"https://video-preview.s3.yandex.net/YjyXDgIAAAA.mp4","videoType":"video/mp4"},"target":"_self","position":"7","reqid":"1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL","summary":{"fullTextUrl":"/int_search_summary?data=http%3A%2F%2Fwww.youtube.com%2Fwatch%3Fv%3DRtT3LiBpZzs","linkTemplate":"/video/preview/5934442990834096176?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=%%timestamp%%&ask_summarization=1"},"isAdultDoc":false,"relatedParams":{"text":"What is SMA Disease and What Are Its Symptoms?","related_orig_text":"sma","related_porno":false,"related_less_3m_off":true,"client":"d2d","no_cnt":1,"related_src":"serp","related":"{\"porno\":false,\"vfp\":1,\"orig_text\":\"sma\",\"url\":\"http:\\/\\/www.youtube.com\\/watch?v=RtT3LiBpZzs\",\"src\":\"serp\",\"rvb\":\"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_AQA-_4C_wME_gH_Bgj_-f7-AO39AQQJAAAA-vX9B_0AAAD1DggA-wAAAPEA-QkBAAAACP8EBAQAAAAM_gT6BwAAAAf88fgAAQAAAwIHAQP_AAAj9_35_wAAAPwC_-4AAAAA8gEF-wAAAAAH-AD-AAAAACAALYjv3js4E0AJSE5QAiqEAhAAGvABf_D7A68b9fxkFQUA2PsDAacS8wD6DQsA0Bn2ANMn5QAH_uoA2-IAABH0DAH8DQv_CO_8_z3-_gAVIRP_LQERANrwHgAO4fMBLQD-AP_23f_6-x4ADgb3ABvf-AEVChn_CRMEAfT6Df0V9AAAE_z_A_EHAP_XAegCGAIC_u4O9QQDCfUAJgcRABr5CQLn_A379fX2_gAFB_z69Aj--gjp_g382v8FAun8EgsaBv_i8_z8AAr4GAYc_Qb57ATs_AX6Jf8c_AgUBQAO-QLyCPn3Cvr-CgT_7Pz6DRr6Bwnn_AIQ-Qb6_AUH-OX6AP7x6RD6IAAtG6hMOzgTQAlIYVACKs8HEAAawAenlcK-vuutPf6jJbzvjNY9egg5PYrJG734g0a9VsGDvO3E-rvpty--efNKPZVjEr29jpC-fOdcvdimKTs5TC89OoQgPftWMD2_Dze-HdloOj0CaT1nJ6O-zhm0uqUmHroQXAU-m5NVu-2sK7sU8py8Ijp_PUzxIr0wO_o8d8RcPT_9ZzwgJfa95jAIO_JPX7yjyIo-qBW7vTzSqjxAg3K8emqaPX8VYLzgoQi-YQRovYosyDylUf273e16PelKwjvjNU8-edrrvINdwzwGSuq9IA60uW-xxzxYNwE8ztKvvXYGvruoazI9AK0ZvVHBHD3GHoU9sA9BPVEejLy5asM8lfW2PIxtLTzkZvg9ZkzhPRgj1DvgoD299ZHlPLhvmjykA6s7xnkOPelHQ7yzn0C9pdGuuxyFHrxCiIW9bT4JPXMmZ7mDbNm8cFMtPazYMjiPri08gjuQvMAfozy1bgO-M8QxvYvlcTxxDIc9NaBZPR2RbztJYUM9GVRgvcXnzjwvr9K8oOL4vK0stLsg1LW9i4lNPI4bADxfY5I9qBp_O2qQODzWk6S9DrErPVaZkbmSMvM8AEs4PV15QbtqMYi99h9evWl0A7nr5v287U-9vBHXnDssvTG9-ow1Pe0IrzolxIY9phhWPdz8-bu0cxo-tuy1PdX3hrjPo-K9Q10_PcfUmrmbG6g9x8mzO06oFjtThiA91i55uz8h-bqIBJ28rPsMPePn2DpBpps9aiSjvQxECbuIeos8dGKsutAObboOZeg8ZonJPfHB8bgNFrM8CHyJPdyp-DhWxUq9zoTsu410gDka-FW7Lrxcve8-uTike0w9PUoAu5IOHzptANa9ohisuvxy2Dip7qs9E8bAPeauPTc-H8q8dVwIPaZ7NLmCdRw9jSLAPW6qOzl4Ik29h44YvT-1hLiBvqE79Q_iPA4lKTlftRq6r89cPRaey7jIKKq85aIQPQynkDhfK1s6pMHNPZL_0ThgJ3C9mhFZPQenmbddrjg7gfOdPbMYYrZG0cO8qk4CvUuVYLjFIDA82Q02POVLODifyR69UhZ0PHQqGjll0Sq92zMbvrJptTjNO4688JFIPV69uThOHXW8kNTnPKPf0TIRw6O9nVWVvGHdmDcNnqM9TsjYvHYfv7i2Mry9321eu0CWI7eXU7e9pCRavGEInLg1fIu8ADy_O-G-PTachsk7cDIAvcMdGTdcWSK71_oivRyhn7cZp8a883t2PFwiv7jhLYu9m3_LOuYACjiBEWo8LfghvORr_jcgADgTQAlIbVABKnMQABpgRgoALQMg-dvqP833KM0BGB73GPTUAP8REgD3QdnC9hjPzPhAAHkVJO6iAAAAMa_e-LQAC3_T9-Y02Q_yw7_MGgZ_FfwR3OMY_pPZtQ0G5OINzWAoAOUSnytR3to3-ScaIAAtPWcQOzgTQAlIb1ACKq8GEAwaoAYAAAhCAACEwgAABMIAAIhBAADIwQAA8EEAAFTCAACAvwAAUMEAAKDCAABAQQAAbMIAALjBAACCwgAAVEIAADzCAADgQAAAEMEAADBBAABAwAAACMIAAADBAADAwQAAFMIAAERCAACwwQAAGMIAABxCAADgQQAAkMEAAEDAAACGQgAAusIAAChCAABQwQAA0EEAAIjBAACgQgAAAMIAAKhBAAC4QQAAQEIAANBBAAB4QgAA-EEAADjCAACIwgAAgEAAAFRCAACawgAA-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-AAAwPQAAcD0AAOi9AAAQPQAAhj4AAKA8AADgPAAADL4AAFC9AABQPQAAJD4AANI-AAB_PwAAqL0AAGQ-AACAuwAAyL0AAEA8AAAwvQAAHD4AAKi9AACIPQAAqD0AAJg9AABAPAAAML0AABQ-AADYvQAAiD0AAJi9AADYvQAAcD0AAJg9AACAuwAAiD0AACS-AAAMPgAAcL0AAOA8AABcvgAARL4AABS-AAAQPQAAVD4AAII-AADIPQAADD4AAFA9AAABPwAAuL0AAMg9AAD4PQAAML0AAEA8AACIvQAAHL4gADgTQAlIfFABKo8CEAEagAIAAEC8AACCPgAAfL4AAEG_AABsvgAAmD0AADM_AAAUvgAA-D0AAKg9AABQPQAArr4AALg9AAB8vgAAXD4AABC9AAAcPgAA1j4AAIK-AACyPgAA4DwAAJg9AAAMvgAABD4AAKA8AAD4PQAA2L0AAKg9AAA8vgAAdL4AAKC8AABQPQAAuL0AAKi9AABMvgAA-L0AAGQ-AABUvgAAZL4AADy-AADovQAARD4AAKg9AAAsPgAAQDwAAPg9AAB_vwAAgDsAAIa-AABQPQAAQDwAAKY-AABAPAAA-D0AAIa-AAA8PgAAUL0AAOg9AACOPgAAiL0AAAw-AABQPQAAqD0AAOA8IAA4E0AJSHxQATAJOAFKAGAAaAA,\"}","related_url":"http://www.youtube.com/watch?v=RtT3LiBpZzs","parent-reqid":"1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-kl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Sağlık Bilimleri Üniversitesi Öğretim Üyesi Çocuk Nöroloji Uzmanı Prof. Dr. Aycan Ünalp, SMA hastalığı hakkında bilinmesi gerekenleri anlattı. SMA hastalığı nedir, neden olur?","preview":{"posterSrc":"//avatars.mds.yandex.net/get-vthumb/760317/7970925ffc31550432d0e01ee4394ce9/564x318_1","videoSrc":"https://video-preview.s3.yandex.net/c9yt4QEAAAA.mp4","videoType":"video/mp4"},"target":"_self","position":"8","reqid":"1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL","summary":{"isFull":true,"fullTextUrl":"/video/result?ask_summarization=1&numdoc=1&noreask=1&nomisspell=1&parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=videoid:594477270930393846","teaser":[{"list":{"type":"unordered","items":["Bu video, bir nöroloji uzmanının Semiha hastalığı hakkında detaylı bilgi verdiği bir sunum formatındadır. Konuşmacı, Beş Çocuk Hastanesi Tıp Fakültesi'nde çalışan bir doktor olarak kendini tanıtmaktadır.","Video, Semiha hastalığının genetik yapısı, sıklığı, tipleri ve tedavi yöntemleri hakkında kapsamlı bilgiler sunmaktadır. Hastalığın beş farklı tipi (tip 1-4) açıklanmakta, her birinin belirtileri ve yaşam beklentisi anlatılmaktadır. Erken tanı ve tedavinin önemi vurgulanırken, şu anda mevcut olan tedavi yöntemleri (Muhsin Ersen) ve evde bakım hizmetleri hakkında bilgiler verilmektedir. Ayrıca, hastalığın genetik geçişli olduğu için evlilik öncesi genetik danışmanlık ve tarama önemi de vurgulanmaktadır."]},"endTime":741,"title":"Semiha Hastalığı Hakkında Bilgilendirici Sunum","beginTime":0}],"fullResult":[{"index":0,"title":"Semiha Hastalığı Hakkında Genel Bilgiler","list":{"type":"unordered","items":["Semiha hastalığı, ilerleyici genetik geçişli alt motor nöronların dejenerasyonu (yıkımıyla) giden kronik bir hastalıktır.","Çocukluk çağında toplumdan topluma değişmekle birlikte 12 binde bir ile 6 binde bir arasında sıklığı değişmektedir.","Akraba evliliğinin sık olduğu toplumlarda (örneğin Türkiye'de) taşıyıcılık oranı 40-45'e bir insanda mutasyon saptanmaktadır."]},"beginTime":5,"endTime":87,"href":"/video/preview/594477270930393846?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=5&ask_summarization=1"},{"index":1,"title":"Genetik Mekanizma ve Tedavi","list":{"type":"unordered","items":["Hastalık genetik geçişli tekken monogenik mutasyonla oluşur ve 5. kromozomda SMN-1 ve SMN-2 adlı iki protein bulunur.","SMN-1 proteini %80-85 oranında üretilirken, SMN-2 daha inaktif formda olur ve SMN-1'in yetersizliği durumunda aktif olur.","SMN-2'nin kopya sayısı önemlidir; 2 ve üzerinde kopya varsa durum daha iyi olur ve şu anda genetik tedavisi mümkün olan hastalıklardan biridir."]},"beginTime":87,"endTime":148,"href":"/video/preview/594477270930393846?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=87&ask_summarization=1"},{"index":2,"title":"Erken Tanı ve Tedavi","list":{"type":"unordered","items":["Teşhis koyup tedavisi olduğu için erken tanı konulup erken tedavinin önemli olduğu bir hastalık grubudur.","İlk 14 gün içerisinde tanı koyduktan sonra tedavisinin başlanması gerekiyor, hatta hamilelikte amniyosentez ile erken tanı konulabilir.","Mevcut olan sağlık bakanlığı'nın izin vermiş olduğu Muhsin Ersen tedavisi beyin omurilik sıvısı içerisine verilir ve belli aralarla testler yapılır."]},"beginTime":148,"endTime":234,"href":"/video/preview/594477270930393846?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=148&ask_summarization=1"},{"index":3,"title":"Hastalık Tipleri","list":{"type":"unordered","items":["Hastalık beş tane tipi vardır: Tip 1 (en kötü hastalık formu, doğum öncesinde hastalık bulgularının başlamış olduğu ve genellikle 2 hafta içerisinde ölümle sonlanan), Tip 2 (6-18 ay arasında bulgu veren), Tip 3 (18 aydan sonra, 2-3 yaştan sonra yürüme bozukluğu, dengesiz yürüme veya sık düşmelerde gelen hastalar), Tip 4 (erişkin yaşlarda güçsüzlükle başlayan).","Tip 3 hastalar SGK ödemesi mevcut olan tedavisi mümkün bir hastalık grubudur.","Erken tanı ve erken ilaca ulaşım bu hastalıkta çok önemlidir."]},"beginTime":234,"endTime":336,"href":"/video/preview/594477270930393846?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=234&ask_summarization=1"},{"index":4,"title":"Hastalığın Klinik Bulguları","list":{"type":"unordered","items":["Hastaların kasları çok güçsüz olduğu için solunum kasları da özellikle erken dönemde etkileniyor ve diyafragmatik solunum, paradoksal solunum (göğsün öne doğru inip çıktığı) görülüyor.","Göğüs kafesi çan zili şeklinde oluyor, skolyoz (belinde eğrilik) ve başını tutamama, oturamama, yürüyememe gibi bulgular görülüyor.","Bilişsel fonksiyonlar tamamiyle normalken vücut motor fonksiyonları geri kalıyor, dilde fasikülasyon (titremeler) olabiliyor ve yürüyüş bozuklukları ortopedik ve fizik tedaviyi ilgilendiren komplikasyonlar meydana getiriyor."]},"beginTime":336,"endTime":439,"href":"/video/preview/594477270930393846?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=336&ask_summarization=1"},{"index":5,"title":"Multidisipliner İzleme ve Bakım","list":{"type":"unordered","items":["Multidisipliner bir izleme önemlidir; fizik tedavi doktoru, ortopedi doktoru, göğüs hastalıkları uzmanı, nefroloji doktoru gerekirse dahil olmalıdır.","Bazı hastalar mekanik ventilatöre bağlı olarak hayatını idame ettirmek zorunda oluyor ve evde bakım hizmetleri mevcuttur.","Tanı konulduktan sonra tedavi aşamasına geçilince palyatif servislerde bu hastaların bakımı yapılabiliyor."]},"beginTime":439,"endTime":484,"href":"/video/preview/594477270930393846?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=439&ask_summarization=1"},{"index":6,"title":"Prognoz ve Tedavi Durumu","list":{"type":"unordered","items":["İlaca iyi cevap veren hastalar oturup yürüme fonksiyonlarını kazanabiliyor, ancak geç teşhis edilirse ve tedaviye geç ulaşılırsa hastalar yatağa bağımlı kalıyor.","Tip 1 hastaların yaşam süresi 2-3-5 yaşlarında maksimum kısalıyor, Tip 2'de daha iyi, Tip 3 ve 4'te çok fazla etkilenmiyor ama yaşam kalitesi düşük oluyor.","Hastalığın mekanizması genetik olarak eksik protein üretimine dayanıyor ve her geçen gün hücre ölümü (apoptosis) oluyor."]},"beginTime":484,"endTime":554,"href":"/video/preview/594477270930393846?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=484&ask_summarization=1"},{"index":7,"title":"Tedavi İmkanları ve Önleme","list":{"type":"unordered","items":["Eskiden tedavisi yokken şimdi birden fazla tedavisi var ve Türkiye'de bir tanesinin geri ödemesi mevcuttur.","Hastaların aileleri büyük güçlük yaşıyor, sağlam bir çocuk sahibi olmak isteyen ailelerin mutlaka genetik danışmanlık almaları gerekiyor.","Evlenmeden önce tarama yapılması çok önemlidir ve hasta bir çocuğu varsa ailelerin en azından senede bir göğüs hastalıkları uzmanı tarafından görülmesi gerekiyor."]},"beginTime":554,"endTime":650,"href":"/video/preview/594477270930393846?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=554&ask_summarization=1"},{"index":8,"title":"Evde Bakım Hizmetleri","list":{"type":"unordered","items":["Evde bakımı mümkün olmadığında palyatif bakım merkezleri ve nöroloji servisleri hastaları yatırıp bakabiliyor.","Evde bakım hizmetlerinden ailelerin bilgi sahibi olması için hastanelere gidip dosya açtırmaları gerekiyor.","Hastaların evine kadar hemşire, sağlık memuru veya bazen doktor arkadaşlar giderek tetkik ve muayeneleri yapıyor, eksik olan cihazları ve raporları hallediyorlar."]},"beginTime":650,"endTime":721,"href":"/video/preview/594477270930393846?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=650&ask_summarization=1"}],"linkTemplate":"/video/preview/594477270930393846?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=%%timestamp%%&ask_summarization=1"},"isAdultDoc":false,"relatedParams":{"text":"SMA hastalığı nedir? 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SMA'nın nasıl bir hastalık olduğunu ve tüm gelişmeleri Duygu Göktürk anlattı. Sosyal medyada da SMA hastaları için pek çok...","preview":{"posterSrc":"//avatars.mds.yandex.net/get-vthumb/1593025/ef6d6932709df6b4e3ea90fe6ccbf853/564x318_1","videoSrc":"https://video-preview.s3.yandex.net/bC3IQQEAAAA.mp4","videoType":"video/mp4"},"target":"_self","position":"10","reqid":"1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL","summary":{"isFull":true,"fullTextUrl":"/video/result?ask_summarization=1&numdoc=1&noreask=1&nomisspell=1&parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=videoid:4464696800745115995","teaser":[{"list":{"type":"unordered","items":["Bu video, GZT tarafından sunulan, SMA (Spinal Muscular Atrophy) hastalığı hakkında bilgilendirici bir içeriktir. Sunucu, sosyal medyada yaygınlaşan SMA hastaları konusundaki bilgi kirliliğini gidermek amacıyla bu videoyu hazırladığını belirtiyor.","Video, SMA hastalığının ne olduğunu, belirtilerini, görülme sıklığını ve tedavi yöntemlerini detaylı şekilde anlatıyor. Özellikle SMA tip bir hastalığının belirtileri, tedavi seçenekleri ve Türkiye'deki durum ele alınıyor. Ayrıca, 2016 yılına kadar tedavisi yapılamayan SMA hastalığının günümüzde genetik terapi ve hücresel değiştirme tedavisi gibi yeni yöntemlerle tedavi edilebileceği, ancak bu tedavilerin pahalı olması nedeniyle ailelerin bağış kampanyaları düzenlediği belirtiliyor. Video, Sağlık Bakanı Dr. Fahrettin Koca'nın yeni bir ilacın onay aldığını ve SGK'nın geri ödeme kapsamına alabileceği açıklamasıyla sonlanıyor."]},"endTime":284,"title":"SMA Hastalığı Hakkında Bilgilendirici Video","beginTime":0}],"fullResult":[{"index":0,"title":"SMA Hastalığı Hakkında Genel Bilgi","list":{"type":"unordered","items":["SMA, nadiren görülen ölümcül bir kas hastalığıdır ve omurilikteki ön boynuz motor sinir hücreleri etkilenir.","Bu rahatsızlıkta kasların kontrolünü sağlayan sinirlerin fonksiyonu için gerekli protein üretimi gerçekleşmez ve istemli kaslarda kuvvetsizlik ve erime görülür.","SMA dünya genelinde on binde bir, Türkiye'de ise altı binde bir görülme sıklığına sahiptir ve her kırk çocuktan biri taşıyıcı olabilir."]},"beginTime":2,"endTime":82,"href":"/video/preview/4464696800745115995?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=2&ask_summarization=1"},{"index":1,"title":"SMA Hastalığının Evreleri ve Belirtileri","list":{"type":"unordered","items":["SMA hastalığının en tehlikelisi SMA tip bir denilen evredir ve belirtileri çocukluk yaşlarından itibaren gözle görülebilir.","Yutkunma ve solunum zorluğu, desteksiz oturamama gibi sorunlar görülür ve hastalığın seyri ne kadar erken ortaya çıkarsa o kadar ağır gerçekleşir.","Altı aylık ve daha küçük bebeklerde ortaya çıkan tip bir SMA, bebek ölümlerinin dünyada en sık görülen sebeplerinden biridir."]},"beginTime":82,"endTime":123,"href":"/video/preview/4464696800745115995?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=82&ask_summarization=1"},{"index":2,"title":"SMA Hastalığının Tedavisi","list":{"type":"unordered","items":["SMA hastalığında kesin tedavinin bulunması için genetik terapi ve hücresel değiştirme tedavisi gibi iki tür çalışma yapılıyor.","2016 yılına kadar tedavisi yapılamayan SMA, 2016 yılında bir ilacın piyasaya çıkmasıyla tedavi edilebilir hale geldi.","Bu ilaç motor nöron ölümlerinin geciktirilmesini hedefliyor ve şu an Türkiye'de SMA'ya yönelik uygulanan tek tedavi yöntemidir."]},"beginTime":123,"endTime":170,"href":"/video/preview/4464696800745115995?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=123&ask_summarization=1"},{"index":3,"title":"Tedavi Maliyeti ve Yeni Gelişmeler","list":{"type":"unordered","items":["Türkiye'de uygulanan tedavi hayat boyu sürmesi gerektiği için aileler çocuklarının tek seferde alınan gen tedavisini tercih ediyor.","Bu ilaç sadece Amerika Birleşik Devletleri ve Avrupa'da uygulandığı için çok pahalı olup, dünyanın en pahalı ilacıdır.","2023 yılının başında SMA hastalığı için üretilen ilk ve tek ağızdan alınan ilaç piyasaya sürüldü, hastalar bu ilacı şurup olarak her gün alarak tedavi 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SMA'nın SMN1 genindeki homozigot mutasyondan kaynaklandığı, toplumda yaklaşık 6000-10000'de bir hastalık olduğu ve Türkiye'de taşıyıcılık oranının 40-60'da bir olduğu belirtilmektedir. Ayrıca, taşıyıcı çiftlerin çocuk sahibi olma ihtimali ve bu durumu önlemek için gebelik öncesi tarama testleri ve pre-implantasyon genetik tanı (PGT) gibi yöntemler önerilmektedir."]},"endTime":203,"title":"Spinal Müsküler Atrofi (SMA) Hastalığı Hakkında Bilgilendirme","beginTime":0}],"fullResult":[{"index":0,"title":"Kas Sistemi ve İşlevi","list":{"type":"unordered","items":["Kas sistemi canlıya hareket yeteneği sağlar; sadece yürüme ve koşma değil, çiğneme, sindirim, nefes alma ve kan dolaşımı gibi işlemler de kas sisteminin görevleri arasındadır.","Vücudumuzun yaklaşık yüzde elli'si kaslardan oluşmakta olup, kasların hareket edebilmesi için sinir hücresi (nöron hücresi) tarafından uyarılması gerekir."]},"beginTime":7,"endTime":54,"href":"/video/preview/4733804334094175326?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=7&ask_summarization=1"},{"index":1,"title":"Spinal Müsküler Atrofi Hastalığı (SMA)","list":{"type":"unordered","items":["Spinal Müsküler Atrofi Hastalığı (SMA), nöronların ilerleyici dejeneratif bir hastalığıdır; nöronların bozulması sonucunda etki ettiği kaslarda atrofi (erime) ve güçsüzlük meydana gelir.","SMA, genetik bir hastalıktır ve SMN1 genindeki homozigot mutasyondan kaynaklanır; DNA'nın her iki ipliğinde bu gen bölgesindeki mutasyonun olması durumunda hastalık ortaya çıkar.","DNA'nın tek ipliğinde SMN1 gen bölgesindeki bozukluk durumunda buna taşıyıcılık denir ve taşıyıcı bireyde herhangi bir hastalık meydana gelmez."]},"beginTime":54,"endTime":115,"href":"/video/preview/4733804334094175326?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=54&ask_summarization=1"},{"index":2,"title":"SMA Hastalığının Sıklığı ve Önleme","list":{"type":"unordered","items":["SMA hastalığının sıklığı toplumdan topluma değişse de altıbin ila onbinde bir civarında görülmektedir; Türkiye'de bu oran altıbinde bir civarındadır.","Türkiye'de yaklaşık kırk ila altmış kişiden birinde SMA taşıyıcılığı gözlenmektedir ve her iki bireyin de taşıyıcı olması durumunda doğacak çocuklarda yüzde yirmibeş ihtimalle hastalık olma durumu mevcuttur.","Çocuk sahibi olmak isteyen çiftlerin gebelik öncesinde veya erken gebelik döneminde SMA taşıyıcılığı tarama testini yaptırmaları önerilmektedir; her iki birey de taşıyıcıysa PGT (pre-implantasyon genetik tanı) önerilmektedir."]},"beginTime":115,"endTime":198,"href":"/video/preview/4733804334094175326?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=115&ask_summarization=1"}],"linkTemplate":"/video/preview/4733804334094175326?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=%%timestamp%%&ask_summarization=1"},"isAdultDoc":false,"relatedParams":{"text":"SMA hastalığı nedir? Kimler taşıyıcıdır? SMA hastalığı önlenebilir 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Bu sinirler, nefes alma, yutma ve kolların ve bacakların hareketi için kasları kontrol eder. (Prof Dr...","preview":{"posterSrc":"//avatars.mds.yandex.net/get-vthumb/1646513/98ef0e9539505d3a2849d709f0615682/564x318_1","videoSrc":"https://video-preview.s3.yandex.net/NHIvDAIAAAA.mp4","videoType":"video/mp4"},"target":"_self","position":"18","reqid":"1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL","summary":{"isFull":true,"fullTextUrl":"/video/result?ask_summarization=1&numdoc=1&noreask=1&nomisspell=1&parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=videoid:12583758999636419437","teaser":[{"list":{"type":"unordered","items":["Bu videoda Dr. Hüseyin Cengiz, SMA (Spinal Musküler Atrofi) hastalığı hakkında bilgi veriyor. ","Video, SMA hastalığının ne olduğunu açıklayarak başlıyor ve ardından evlenmeden önce veya gebe kalmadan önce SMA hastalığı riskini nasıl anlayabileceğimizi anlatıyor. SMA'nın genetik olarak aktarılan otozom resesif bir hastalık olduğu, anne ve babanın taşıyıcı olması durumunda bebeğin SMA'lı olma ihtimalinin 6-10 binde bir olduğu belirtiliyor. Dr. Cengiz, anne adayında taşıyıcılık taraması yapılabileceğini, ideal olarak gebelik öncesi yapılması gerektiğini ve artık 81 ilde evlilik öncesi ücretsiz SMA taşıyıcılık taraması yapılacağını paylaşıyor."]},"endTime":352,"title":"SMA Hastalığı ve Taşıyıcılık Taraması","beginTime":0}],"fullResult":[{"index":0,"title":"Spinal Musküler Atrofi (SMA) Hastalığı","list":{"type":"unordered","items":["SMA (Spinal Musküler Atrofi) hastalığı, sinir kas hastalığı olup omurilikteki motor nöronları harap ederek ilerleyen ve ölüme kadar yol açabilen bir durumdur.","SMA hastalığı genetik olarak aktarılan otozom resesif kalıtılan bir hastalık olup, doğacak bebeğin hem annenin hem babada taşıyıcılığı olması gerekir.","SMA'lı bir çocuk doğma ihtimali altı binde bir ile on binde bir arasında düzenlenmektedir."]},"beginTime":7,"endTime":90,"href":"/video/preview/12583758999636419437?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=7&ask_summarization=1"},{"index":1,"title":"Taşıyıcılık Taraması","list":{"type":"unordered","items":["Taşıyıcılık taraması sadece anne adayında yapılabilir ve taşıyıcılık oranı elli'de bir civarındadır.","Taşıyıcı bir anne adayı ve taşıyıcı bir baba adayı evlendiğinde, SMA'lı bir çocuk sahibi olma olasılıkları dörtte birdir.","Türkiye'nin coğrafi konumu ve akraba evliliklerinin yüksek olması nedeniyle bu hastalık nispeten daha sık görülmektedir."]},"beginTime":90,"endTime":154,"href":"/video/preview/12583758999636419437?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=90&ask_summarization=1"},{"index":2,"title":"Taşıyıcılık Testi","list":{"type":"unordered","items":["Bebek sahibi olmak isteyen herkese gebelikten önce taşıyıcılık testi yapılabilir, ideal olanı gebelikten önce bakmaktır.","Taşıyıcılık testi basit bir kan testi ile yapılabilir ve maliyeti vardır.","Tarama testi negatif ise, SMA'lı bir çocuk sahibi olma olasılığı çok düşüktür (bazı kaynaklarda %98 gibi görülüyor)."]},"beginTime":154,"endTime":221,"href":"/video/preview/12583758999636419437?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=154&ask_summarization=1"},{"index":3,"title":"Ulusal Taşıyıcılık Taraması","list":{"type":"unordered","items":["Bakanlık, evlenmeden önce çiftlere 81 ilde ulusal SMA taşıyıcılık taraması planlamıştır.","Ekim ayında ihale yapılarak SMA kitleri alınmış ve isteyen çiftlere, anne adaylarına evlenmeden önce SMA testi ücretsiz olarak yapılacak.","Taşıyıcılık testi sonucunda hem kadın hem erkek taşıyıcıysa, SMA'lı bir bebek sahibi olma ihtimali dörtte birdir ve genetik danışmanlık gereklidir."]},"beginTime":221,"endTime":317,"href":"/video/preview/12583758999636419437?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=221&ask_summarization=1"},{"index":4,"title":"Sonuç ve Öneriler","list":{"type":"unordered","items":["SMA'lı bir bebek sahibi olmak istemiyorsanız, gebelikten önce mümkünse hamilelikten önce bu testi yaptırmanız önerilir.","Eğer bu aşamaları atlamışsak da hamileyken de bu testi yaptırmanız mümkündür.","Taşıyıcılık testi basit bir kan testi olup, değerlendirilebilir bir seçenektir."]},"beginTime":317,"endTime":351,"href":"/video/preview/12583758999636419437?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=317&ask_summarization=1"}],"linkTemplate":"/video/preview/12583758999636419437?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=%%timestamp%%&ask_summarization=1"},"isAdultDoc":false,"relatedParams":{"text":"SMA (Spinal Muskuler Atrofi) Hastaliği Taramasi? 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Spinal Musküler Atrofi (SMA) hastalığına yakalanan bir bebek ya da bir çocuk için düzenlenen bağış kampanyalarına son dönemde çok sık rastlanıyor. Aileler, Zolgensma isimli \"dünyanın...","preview":{"posterSrc":"//avatars.mds.yandex.net/get-vthumb/3591199/e534eba0ba2b36ec2fcaac14cb2e6770/564x318_1","videoSrc":"https://video-preview.s3.yandex.net/8oCqVwEAAAA.mp4","videoType":"video/mp4"},"target":"_self","position":"19","reqid":"1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL","summary":{"isFull":true,"fullTextUrl":"/video/result?ask_summarization=1&numdoc=1&noreask=1&nomisspell=1&parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=videoid:3129619004848597729","teaser":[{"list":{"type":"unordered","items":["Bu video, SMA (Spinal Muscular Atrophy) hastalığı ve Zolgensma gen tedavisi hakkında bilgilendirici bir içeriktir. Videoda Sağlık Bakanı Fahrettin Koca'nın görüşleri de yer almaktadır.","Video, SMA hastalığının ne olduğunu, Zolgensma tedavisinin nasıl çalıştığını ve bu tedavinin dünyanın en pahalı ilacı olduğunu anlatmaktadır. Tedavi için gerekli olan 2,40 milyon dolar maliyeti, bazı ailelerin çocuklarını tedavi etmek için para toplamak zorunda kalması ve Türkiye'deki durum ele alınmaktadır. Ayrıca, ilacın yan etkileri, tedavi için gerekli yaş ve kilo sınırları ve sağlık bakanının \"kirli kampanya\" ifadesi de videoda yer almaktadır."]},"endTime":450,"title":"SMA Hastalığı ve Zolgensma Tedavisi Hakkında Bilgilendirici Video","beginTime":0}],"fullResult":[{"index":0,"title":"Sma Hastalığı ve Tedavi İhtiyacı","list":{"type":"unordered","items":["Sma (Spinal Muscular Atrophy) hastalığı için gen tedavisi gerekiyor ve şu an bir ilaç var.","Sma, bebeklerde en sık görülen kalıtımsal hastalığa bağlı ölüm sebebidir ve tüm dünyada sayısız aile bu hastalıkla mücadele etmektedir.","2019'da ABD'de kullanımı onaylanan Zolgensma isimli ilaç, Sma'nın en ağır türleri için umut olmuştur."]},"beginTime":5,"endTime":61,"href":"/video/preview/3129619004848597729?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=5&ask_summarization=1"},{"index":1,"title":"Tedavi Süreci ve Zorluklar","list":{"type":"unordered","items":["Sma hastalığında SMN1 geni çalışmıyor ve tedavi, bu çalışmayan geni hastalara vererek yapılıyor.","Tedavi, çocuk iki yaş ve belli bir kilodan önce uygulanmalı, aksi takdirde ilaç etkili olmayabilir.","Bazı çocukların durumu çok hızlı ilerliyor ve kas erimesi arttıkça tedavinin etkisi azalıyor."]},"beginTime":61,"endTime":128,"href":"/video/preview/3129619004848597729?parent-reqid=1776721486398476-14570141139016972738-balancer-l7leveler-kubr-yp-klg-246-BAL&text=sma&t=61&ask_summarization=1"},{"index":2,"title":"İlaç Fiyatı ve Tartışmalar","list":{"type":"unordered","items":["İsviçreli Novartis firması tarafından üretilen Zolgensma, 2 milyon doların üzerindeki fiyatıyla dünyanın en pahalı ilacıdır.","Şirket, yüksek maliyeti tedavi sürecinin normal şartlarda seneler sürmesi ve milyonlarca euro'ya mal olması nedeniyle savunmaktadır.","Amerika hükümeti yarım milyar dolara yakın para vererek temel araştırmalara katkı 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