PROGERIYA
DOI:
https://doi.org/10.37547/Keywords:
Progeriya, tez qarish, genetik kasallik, LMNA geni, hujayra mutatsiyasi, o‘sishning sust rivojlanishi, teri va soch holati, mushak va bo‘g‘im zaifligi, yurak-qon tomir kasalliklariAbstract
Progeriya — bu kam uchraydigan genetik kasallik bo‘lib, bemorlarning tanasi va hujayralari tez qarish jarayoniga duchor bo‘ladi. Kasallik odatda LMNA geni mutatsiyasi bilan bog‘liq bo‘lib, bu hujayralarning normal funksiyasini buzadi. Progeriyaga chalingan bolalarda o‘sish sekinlashadi, teri va sochning holati yomonlashadi, mushak va bo‘g‘imlar zaiflashadi hamda yurak-qon tomir kasalliklari rivojlanadi. Hozirda progeriyani to‘liq davolash yo‘q, ammo simptomlarni kamaytirish va bemorning hayot sifatini yaxshilash mumkin.
Downloads
References
1.Wang-Michelitsch, J., & Michelitsch, T. M. (2015). Premature aging as a consequence of Mis-construction of tissues and organs during body development. arXiv.
2.Shahzod Gafforov. (2024). Erta qarish sindromiga chalingan erkak 28 yoshida vafot etdi. Yuz.uz.
3.Alldata. (n.d.). O'zbekistonda yuqori texnologiyalarga asoslangan ishlab chiqarishni rivojlantirish yo'nalishlari mavzusi uchun kirish, xulosa va foydalanilgan adabiyotlar ro'yxati. Alldata.uz.
4.Alldata. (n.d.). Xulosa chiqarishning tuzulishi. Alldata.uz.
5.Alldata. (n.d.). Aholining turmush farovonligini oshirish yo'llari mavzusi bo'yicha kirish, xulosa va foydalanilgan adabiyotlar ro'yxati. Alldata.uz..
Downloads
Published
Issue
Section
License

This work is licensed under a Creative Commons Attribution 4.0 International License.
Articles published in this journal are licensed under the Creative Commons Attribution 4.0 International License (CC-BY 4.0). Under this license:
- Share: Copy and redistribute the material in any medium or format
- Adapt: Remix, transform, and build upon the material for any purpose, including commercially
Attribution required: You must give appropriate credit, provide a link to the license, and indicate if changes were made.
License URL: https://creativecommons.org/licenses/by/4.0/
Authors retain copyright of their work while granting the journal first publication rights.