Please use this identifier to cite or link to this item: http://repo.tma.uz/xmlui/handle/1/2497
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dc.contributor.authorAbdulxamidova D.L., Abdurahmonova H.N., Omonov Sh.R.-
dc.date.accessioned2025-12-05T06:36:35Z-
dc.date.available2025-12-05T06:36:35Z-
dc.date.issued2025-
dc.identifier.urihttp://repo.tma.uz/xmlui/handle/1/2497-
dc.description.abstractMegaloblastik makrositar anemiya – bu DNK sintezining buzilishi natijasida yuzaga keladigan va megaloblastik eritropoez bilan xarakterlanuvchi kasallikdir. Ushbu anemiya asosan B12 vitamini yoki foliy kislotasi tanqisligi bilan bog‘liq bo‘lib, eritropoez jarayonida patologik o‘zgarishlar keltirib chiqaradi. Suyak iligi giperkellular bo‘lib, megaloblastik hujayralarning ortiqcha to‘planishi kuzatiladi. Periferik qonda makrositar eritrositlar, anizositoz, poikilositoz va gipersegmentatsiyalangan neyrofillar aniqlanadi. Klinik jihatdan bemorlarda umumiy holsizlik, nevrologik buzilishlar, dispeptik sindrom va oshqozon-ichak traktining shikastlanishlari kuzatiladi. Ushbu maqolada megaloblastik anemiyaning patologik anatomiyasi, etiologiyasi, klinik ko‘rinishlari va diagnostik yondashuvlari muhokama qilinadi.en_US
dc.language.isootheren_US
dc.publisherO'zbekiston, Toshkenten_US
dc.subjectMegaloblastik anemiya, makrositar anemiya, B12 vitamini, foliy kislotasi, eritropoez, gipersegmentatsiyalangan neyrofillar.en_US
dc.titleMEGALOBLASTIK MAKROSITAR ANEMIYAen_US
dc.typeArticleen_US
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