BOLALARDAGI TURLI POLINEYROPATIYALAR TASHXISOTIDA MULTIMODAL YENDOSHUV
Abstrakt
Dolzarbligi: Bolalardagi polinevropatiyalar turli xil sabablar, yoshga xos klinik ko‘rinishlar va maxsus baholash usullarini talab qilishi tufayli tashxis qo‘yishda qiyinchiliklar tug‘diradi. Klinik baholash, elektrofiziologiya, laboratoriya tekshiruvlari va tasvirlash usullarini o‘z ichiga olgan ko‘p qirrali diagnostika yondashuvi aniq tashxis qo‘yish va davolash uchun juda muhimdir. Maqsad: Bolalar polinevropatiyalarini aniqlashda tuzilmaviy ko‘p qirrali tashxislash yondashuvining samaradorligini baholash va turli usullarning tashxislash natijadorligini aniqlash. Tadqiqot materiallari va usullari: Farg‘ona viloyat bolalar ko‘p tarmoqli tibbiyot markazida polinevropatiyaga shubha qilingan 85 nafar pediatrik bemorda (0-18 yosh oralig‘ida) retrospektiv tahlil o‘tkazildi. Diagnostika protokoli keng qamrovli klinik baholash, nerv o‘tkazuvchanligini tekshirish (NKS) va elektromiografiya (EMG), maqsadli laboratoriya tekshiruvlari, neyrotasvirlash va ko‘rsatma bo‘lganda genetik tekshiruvlarni o‘z ichiga olgan. Tadqiqot natijalar: 78 nafar bemorda (91,8%) aniq tashxis qo‘yildi. Eng keng tarqalgan sabablar irsiy neyropatiyalar (34,1%), immunitet bilan bog‘liq yallig‘lanish neyropatiyalari (28,2%) va metabolik o‘zgarishlar (15,3%) edi. Nerv o‘tkazuvchanligini o‘rganish eng yuqori tashxislash natijasini ko‘rsatdi (89,4%), keyingi o‘rinlarda maqsadli genetik tekshiruvlar (irsiy holatlarda 72,3%) va laboratoriya tekshiruvlari (68,2%) turadi. Xulosalar: Tuzilgan ko‘p usullik yondashuv bolalardagi polinevropatiyalarni aniqlash aniqligini sezilarli darajada oshiradi. Elektrofiziologik tekshiruvlarni erta qo‘llash, maqsadli laboratoriya va genetik sinovlar bilan birgalikda, o‘z vaqtida tashxis qo‘yish va tegishli choralar ko‘rishni ta’minlaydi.
Mualliflar haqida
Adabiyotlar ro'yxati
Babaee, M., & Fatehi, F. (2023). What is the next step after an electrodiagnostic study in children with polyneuropathies? Rationale for laboratory and other diagnostic tests. International Journal of Child Neurology. https://pmc.ncbi.nlm.nih.gov/articles/PMC10704288/
Dikmen, P. Y. (2018). Electromyography in pediatric population. Archives of Neuropsychiatry. https://pmc.ncbi.nlm.nih.gov/articles/PMC6045805/
Grew, S., Gianneschi, F., & Elgallab, A. (2025). Chronic inflammatory demyelinating polyneuropathy following natural influenza A infection in a pediatric patient: A case report and literature review. Case Reports in Neurological Medicine, 2025, Article 8840308. https://doi.org/10.1155/crnm/8840308
Kumar, S., Meister, A., Narendran, N., & Lee. (2025). The incidence and burden of peripheral neuropathy in pediatric oncology patients receiving levofloxacin and vincristine compared with vincristine alone. Journal of Pediatric Hematology/Oncology. https://doi.org/10.1097/MPH.0000000000003103
Gnanakumar, S., et al. (2025). Peripheral neuropathy as an early marker in newborn-screened Krabbe disease: The value of pre-confirmatory neurophysiological testing. Journal of the Peripheral Nervous System. https://doi.org/10.1111/jns.70040
Ahmad, N. (2019). Outcome of neuromuscular electrodiagnostic testing in children. Journal of the College of Physicians and Surgeons Pakistan. https://www.jcpsp.pk/article-detail/poutcome-of-neuromuscular-electrodiagnostic-testing-in-childrenorp
İpek, G., et al. (2025). Genotypic and phenotypic characterization of axonal Charcot-Marie-Tooth disease in childhood: Identification of one novel and four known mutations. Genes, 16(8), 917. https://doi.org/10.3390/genes16080917
Jaubert, L., et al. (2025). Nationwide phenotypic and genotypic characterisation of 103 patients with SH3TC2 gene-related demyelinating peripheral neuropathy. European Journal of Neurology. https://doi.org/10.1111/ene.70313
Gross, A., Berger, M., Neunhoeffer, S., Nordmeyer, T., & Bevot, J. (2025). Case report: Post-surgical Guillain-Barré syndrome as a rare differential diagnosis of flaccid paralysis of the lower extremities in an infant after cardiac surgery. Frontiers in Pediatrics, 13, 1610035. https://doi.org/10.3389/fped.2025.1610035
Khadra, A., et al. (2025). From initial suspicion to accurate diagnosis: Unmasking rabies in a case of suspected Guillain-Barre syndrome. BMC Pediatrics, 25, 5994. https://doi.org/10.1186/s12887-025-05994-x
Yépez, V. A., et al. (2025). The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease. Nature Genetics. https://doi.org/10.1038/s41588-025-02290-3
Choi, G., Fu, Yan, & Li. (2025). Ofatumumab for the treatment of anti-neurofascin 155 autoimmune nodopathy: A case series. Brain and Behavior. https://doi.org/10.1002/brb3.70717
Alsaadi, T., et al. (2018). Clinical and electrophysiological features of pediatric Guillain-Barré syndrome in the United Arab Emirates. Neurosciences, 23(4), 289-295.
Cornblath, D. R., et al. (2019). Research criteria for diagnosis of chronic inflammatory demyelinating polyneuropathy (CIDP). Neurology, 93(21), 920-930.
Eggermann, K., et al. (2018). Hereditary neuropathies. Deutsches Ärzteblatt International, 115(6), 91-97.
Grüter, T., et al. (2020). Clinical and neurophysiological features of early-onset Charcot-Marie-Tooth disease. European Journal of Paediatric Neurology, 24, 155-162.
Hansson, B., et al. (2021). Genetic testing in pediatric peripheral neuropathy: A systematic approach and diagnostic yield. Pediatric Neurology, 115, 45-52.
Jones, H. R., et al. (2019). Pediatric electromyography: Techniques, normal values, and clinical applications. Muscle & Nerve, 59(2), 162-172.
Kolb, S. J., & Kissel, J. T. (2015). Spinal muscular atrophy. Neurologic Clinics, 33(4), 831-846.
Lawson, V. H., & Gordon Smith, A. (2007). The natural history of chronic inflammatory demyelinating polyneuropathy in childhood. Pediatric Neurology, 37(4), 273-278.
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