a novel cybb mutation in chronic granulomatous disease in iran

نویسندگان

shaghayegh tajik immunology, asthma and allergy research institute, tehran university of medical sciences, tehran, iran

mohsen badalzadeh immunology, asthma and allergy research institute, tehran university of medical sciences, tehran, iran

mohammad reza fazlollahi immunology, asthma and allergy research institute, tehran university of medical sciences, tehran, iran

massoud houshmand department of medical genetics, national institute of genetic engineering and biotechnology (nigeb), tehran, iran

چکیده

chronic granulomatous disease (cgd) is a rare primary immunodeficiency disorder due to a genetic defect in one of the components of nicotinamide adenine dinucleotide phosphate (nadph) oxidase complex. this complex is composed of membrane-bound gp91- phox and p22- phox subunits, and cytosolic subunits consisting of p47- phox , p67- phox , and p40- phox . a mutation in cybb gene encoding gp91- phox located on chromosome xp21.1, leads to x-linked cgd. herein, we report a 4-year-old iranian boy presented with episodes of recurrent fever, cervical lymphadenopathy, and abdominal abscesses. mutation analysis of the cybb gene in the patient indicated a one-nucleotide deletion, c.316delt, resulting in p.w106gfsx.

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عنوان ژورنال:
iranian journal of allergy, asthma and immunology

جلد ۱۵، شماره ۵، صفحات ۴۲۶-۴۲۹

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