POLYURIYA VA RAXIT SINDROMI BILAN KECHUVCHI TUBULOPATIYA KLINIK HOLATI (gipofosfatemik raxit?)
Abstrakt
Muvofiqlik. Tubulopatiyalar - bu elektrolitlar, minerallar, suv va organik moddalarning quvurlar orqali o'tishining turli xil buzilishlari, irsiy (birlamchi tubulopatiyalar) yoki orttirilgan (ikkilamchi tubulopatiyalar) bilan tavsiflangan quvurli buyrak kasalliklari. Bular poliuriya, polidipsiya, skelet deformatsiyasi va surunkali buyrak etishmovchiligining (CRF) mumkin bo'lgan rivojlanishi kabi alomatlar bilan klinik jihatdan namoyon bo'ladigan holatlardir. Turli sabablar va noyob mexanizmlarga qaramay, bemorlarni o'z vaqtida tashxislash, davolash va reabilitatsiya qilish masalalari hal etilmagan.Tadqiqot maqsadi. skelet deformatsiyasi va poliuriya bilan og'rigan tubulopatiya bilan og'rigan bemorning klinik holatining tavsifi. Tadqiqot materiali va usullari. Ushbu maqolada biz O‘zbekiston Respublikasi Farg‘ona vodiysida bolalar o‘rtasida aniqlangan poliuriya va gipofosfatemik raxit ko‘rinishlari bilan og‘rigan irsiy tubulopatiya bilan og‘rigan bemorning o‘z klinik kuzatuvlarimiz bilan o‘rtoqlashmoqchi edik.Tadqiqot natijalari. Bemor S.ning klinik holati shuni koʻrsatdiki, kech tashxis qoʻyilganligi va davolashni kech boshlaganligi sababli bemorda oʻsishning kechikishi, skelet deformatsiyasi, shuningdek, suvsizlanish va atsidoz rivojlangan. Xulosa. Bolalardagi tubulopatiyalarni davolashda, ayniqsa, surunkali buyrak kasalligi bo'lgan oilalarda erta aniqlash va genetik maslahat muhim ahamiyatga ega. Molekulyar genetik tadqiqot o'tkazish bemorni davolash bo'yicha taktik qadamlarni rejalashtirish va keyinchalik ma'lum bir oilada tubulopatiyali bolalar tug'ilishining oldini olish imkonini beradi.
Nashr sanasi
Mualliflar haqida
Adabiyotlar ro'yxati
Miftakhova A.M. "Phosphate diabetes clinical case of familial hypophosphatemic rickets". Perm State Medical University named after academician E.A. Wagner, Russia 2023 pp. 142-150.
Rakhmanova L.K., Majidova N.M. Regional features of the course and prevention of Lowe syndrome in children // Tashkent tibbiyot akademiyasi Axborotnomasi (O’zbekiston). 2024- №9.P.158-163.
Majidova N.M., Rakhmanova L.K., Ganieva M.Sh., Clinical cases of hereditary tubulopathies in children in the Fergana Valley of Uzbekistan // Bulletin of the Tashkent Medical Academy (Uzbekistan). 2024- №7.P.103-108 Part II.
Zh.G. Leviashvili, N.D. Savenkova, I.V. Anichkova. Features of kidney pathology in children with Lowe syndrome. ISSN 1561_6274. Nephrology. 2015. Vol. 19. №6.pp. 53-60.
Ignatova M.S., Korovina N.A. Diagnostics and treatment of nephropathy in children. - M. Geotar-Media, 2007. - 336 p.
Ignatova M.S., Tsalikova F.D. Hereditary nephritis (Alport syndrome). Nephrology. Handbook for doctors. Ed. I.E. Tareeva. M: Medicine 2000; 340-345. (Ignatova M.S., Calikova F.D. Hereditary nephrite. (Alport syndrome) In: Nephrology. I.E. Tareeva (ed). M: Medicina 2000; 340-345.)
Papajan AV, Savenkova ND, Leviashvili ZhG. Hereditary de Toni – Debre – Fanconi syndrome. V: Clinical nephrology of childhood. Levsha. Sankt-Peterburg, SPb, 2000; 208-218].
Barnett H.L., Schoeneman M., Bernstein J. et al. // Pediatric Kidney Disease // Ed. C.M. Edelmann. – Boston, 2009. – P.675.
Jinwoon Joung1 , Heeyeon Cho1 1Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea. Tubulopathy: the clinical and genetic approach in diagnosis.
Rakhmanova L. K., N.M. Madjidova, M.Sh. Ganiyeva. Risk factors for Low syndrome in children. International Conference on Advance Research in Humanities, Sciences and Education AUSTRALIA, CONFERENCE https://confrencea.org JULY15th 2023 стр 137-139 . https://confrencea.org
How to Cite

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.