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  • Clinical case of аtypical hemolytic uremic syndrome

    Редакция | 2013, PM Pediatrics. Clinical observations, Practical medicine 06 (13) Pediatrics | 25 ноября, 2013

    T.P. MAKAROVA, G.R. DAVLETBAEVA, L.V. PОLADOVA, N.V. OSIPOVA, Yu.S. MELNIKOVA
    Kazan State Medical University
    Children’s Republican Clinical Hospital

    Makarova Tamara Petrovna
    Doctor of Medical Science, Professor at the Department of Hospital Pediatrics
    49 Butlerova Str., Kazan 420012
    tel. (843) 237-30-37, e-mail: [email protected] 

    The article contains the results of a clinical supervision of a patient with atypical hemolytic uremic syndrome, receiving therapy with Еculizumab. The clinical characteristics of the disease and the dynamics of laboratory data in the course of treatment is given.

    Key words: аtypical hemolytic uremic syndrome, plasmotherapy, hemodialysis, eculizumab, clinical case.

     

     

    REFERENCES

    1. Popa A.V., Lifshic V.I., Jemirova H.M., Abaseeva T.Ju. i dr. Sovremennye predstavlenija ob atipichnom gemolitiko-uremicheskom sindrome (NON-Stx-HUS) // Pediatrija. — 2011. — T. 90, № 4. — S. 134-140.

    2. Makarova T.P., Jemirova H.M., Zverev D.V., Osipova N.V. Atipichnyj gemolitiko-uremicheskij sindrom u detej // Prakticheskaja medicina. — 2012. — №7 (62). — S. 57-61.

    3. Loirat C., Noris M., Fremeaux-Bacchi V. Complement and the atypical hemolytic uremic syndrome // Pediatr Nephrol. — 2008. — Vol. 23. — R. 1957-1972.

    4. Ariceta G., Besbas N., Johnson S., Karpman D. et al. Guidelines for the investigation and initial therapy of diarrhea negative haemolytic uraemic syndrome // Pediatr Nephrol. — 2009. — Vol. 24. — R. 687-696.

    5. Taylor C.M., Machin S., Wigmore S.J., Goodship T.H. Clinical Practice Guidelines for the management of atypical Haemolytic Uraemic Syndrome in the United Kingdom // Br J Haematol. — 2010. — 148. — R. 37-7

     

    Метки: Clinical case, Eculizumab, G.R. Davletbaeva, Hemodialysis, L.V. Pоladova, N.V. OSIPOVA, Plasmotherapy, Practical medicine 06 (13) Pediatrics, T.P. MAKAROVA, YU.S. Melnikova

    ‹ Diagnosis and treatment of Kasabach – Merritt syndrome in children of one year old Clinical observation of a patient with autosomal-recessive polycystic kidney disease ›
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