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БОЛАЛАРДА ЦЕРЕБРАЛ ИНСУЛЬТ РИВОЖЛАНИШИНИНГ КЛИНИК ХУСУСИЯТЛАРИ ВА МОЛЕКУЛЯР-ГЕНЕТИК МЕХАНИЗМЛАРИ

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Церебро-васкуляр патология болалар неврологиясида энг қизиқарли ва ўрганилган муаммолардан бири бўлиб, уларнинг ахамияти турли ёшдаги болаларнинг юқори даражадаги ногиронлик ва ўлим кўрсаткичлари билан белгиланади. Жахон тиббиётининг даражаси генлардаги мутациялар мавжудлигини истисно этадиган ёки тасдиқлайдиган генетик тадқиқотлар босқичига етди. Болаларда инсульт касаллагининг кўплаб сабаблари орасида генетик мойиллик хам такидланди, [Simma 2010; Zadro 2012; Balzerich, 2018], шунингдек катталар хам бундан мустасно эмас. Ушбу мақолада болаларда инсультнинг этиологияси,таснифи, клиникаси ва молекуляр генетик тадқиқотларига багишланган замонавий адабиётлар тахлили келтирилган. Тадқиқотлар шуни кўрсатадики, инқирозга мойил бўлган номзод генларни аниқлаш ушбу муаммонинг тадқиқотчилари учун устувор вазифалардандир.

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# дети# children# болалар# ischemic stroke# hemorrhagic stroke# ишемик инсульт# геморрагик инсульт# ишемический инсульт# геморрагический инсульт# gene# гомоцистеин# homocysteine# ген

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