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nephrotic syndrome and recurrent infection
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نویسنده
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shahraki ghadimi zahra ,sadeghi bojd simin ,parvaneh nima ,atabaki mehdi ,alijani ebrahim
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منبع
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iranian journal of allergy, asthma and immunology - 2024 - دوره : 23 - شماره : 5 - صفحه:594 -599
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چکیده
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Nephrotic syndrome is characterized by the leakage of protein from the blood into the urine along with the triad of proteinuria, albuminuria, and peripheral edema. loss of protein leads to the loss of immunoglobulin and complements. x-linked agammaglobulinemia (xla), or bruton disease, is a primary immunodeficiency disease caused by a defect in the development of b cells in the bone marrow and a low serum level of immunoglobulins. the present case involves a 12-year-old boy with nephrotic syndrome, osteomyelitis, and recurrent infections. we discovered that he had xla. this report underscores the importance of considering inborn errors of immunity in cases of protein loss, such as nephrotic syndrome.
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کلیدواژه
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bruton type agammaglobulinemia; inborn errors of immunity; nephrotic syndrome; primary immunodeficiency diseases; x-linked agammaglobulinemia
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آدرس
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zahedan university of medical sciences, clinical immunology research center, iran, zahedan university of medical sciences, research institute of cellular and molecular sciences in infectious diseases, ali ibne abitaleb hospital, iran, tehran university of medical sciences, research center for immunodeficiencies, childrens medical center hospital, iran, zahedan university of medical sciences, clinical immunology research center, iran, zahedan university of medical sciences, clinical immunology research center, iran
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پست الکترونیکی
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ebrahimalijani@yahoo.com
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Authors
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