*Five Years Citation in Google scholar (2016 - 2020) is. 1451*   *    IJPR IS INDEXED IN ELSEVIER EMBASE & EBSCO *       

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INTERNATIONAL JOURNAL OF PHARMACEUTICAL RESEARCH

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Published by : Advanced Scientific Research
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0975-2366
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IJPR 9[3] July - September 2017 Special Issue

July - September 9[3] 2017

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Granulomatosis with Polyangiitis: Diagnostic Difficulties and Treatment

Author: MASHKURA RIZAMUKHAMEDOVA, DILDORA NABIYEVA, ELNORA DZHURAYEVA, DILFUZA BERDIEVA, SEVARA MUKHAMMADIEVA
Abstract: The article presents up-to-date data on etiopathogenesis, clinic, diagnostics, differential diagnostics, treatment and prognosis in granulomatosis with polyangiitis (GPA). Early diagnosis of GPA is a difficult clinical task and requires careful examination of the patient using modern research methods to identify pathognomic symptoms. Early detection of anti-neutrophil cytoplasmic antibodies (ANCA) increases the frequency of GPA diagnosis, a biopsy of affected organs allows verifying the diagnosis morphologically. Only timely establishment of the diagnosis allows prescribing therapy as early as possible and avoiding disability of patients.
Keyword: systemic vasculitis, anti-neutrophil cytoplasmic antibodies, granulomatosis with polyangiitis, diagnosis, treatment.
DOI: https://doi.org/10.31838/ijpr/2020.12.02.0112
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