Farmonova, Ruxshona and Daminov, Muslimbek (2023) PATAU SINDROMINING KELIB CHIQISH SABABLARI. Journal of Universal Science Research; Vol. 1 No. 2 (2023): Journal of Universal Science Research (JUSR); 523-528.
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Abstract
Patau sindromi – xromosoma anomaliyasi bu 13-juft autosomada trisomiya. Patau sindromi tibbiyot adabiyotlarida trisomiya D va trisomiya 13 nomlari bilan ham uchrashi mumkin. Kasallikning belgilari: oldingi miya, o`rta yuz zonasi va ko`zlarning anomal rivojlanishi, og`ir aqliy zaiflik, yurak nuqsonlari, tug`ilish paytida kichik o`lchamda bo`lishi bilan namoyon bo`ladi. Patau sindromi bo`lgan bolalarning 95% bachadonda (tug`ilishdan oldin) vafot etadi. Tirik tug`ilgan bolalarning 6-12% bir yildan ko`proq yashagan. Rivojlangan mamlakatlarda 2-3% bolalar 10 yoshga to`lgan.
| Item Type: | Article |
|---|---|
| Additional Information: | Imported from Journal of Universal Science Research |
| SWORD Depositor: | Admin User |
| Depositing User: | Admin User |
| Date Deposited: | 23 Sep 2026 22:40 |
| Last Modified: | 23 Sep 2026 22:40 |
| URI: | https://universalpublishings.uz/id/eprint/5103 |
