[
    {
        "id": "osp-1520",
        "type": "article-journal",
        "title": "Hypocomplementemic Urticarial Vasculitis Syndrome in an 8-year-old Boy: A Case Report and Review of Literature",
        "author": [
            {
                "family": "Al Mosawi",
                "given": "Zakiya Saleh Adnan"
            },
            {
                "family": "Al Hermi",
                "given": "Badriya Ebrahim Ahmed"
            }
        ],
        "URL": "https://omanscience.com/en/articles/hypocomplementemic-urticarial-vasculitis-syndrome-in-an-8-year-old-boy-a-case-report-and-review-of-literature",
        "language": "en",
        "issued": {
            "date-parts": [
                [
                    2013
                ]
            ]
        },
        "container-title": "Oman Medical Journal",
        "DOI": "10.5001/omj.2013.76",
        "publisher": "Oman Medical Specialty Board",
        "ISSN": "1999-768X",
        "abstract": "Hypocomplementemic urticarial vasculitis syndrome is an immune complex-mediated disease of unknown etiology. The clinical course is characterized by urticaria, conjunctivitis, joint pain, and hypocomplementemia. We here report a case of a child with hypocomplementemic urticarial vasculitis syndrome that progressed to nephritis. Renal biopsy was consistent with diffuse proliferative glomerulonephritis with diffuse subendothelial immune deposits. He responded well to a combination of steroid and mofetil micofenolate."
    }
]