نتایج جستجو برای: primary immunodeficiency disease

تعداد نتایج: 2088150  

Journal: :Indian Journal of Paediatric Dermatology 2017

Journal: :Bangladesh Journal of Child Health 2013

Journal: :Journal of Clinical Pathology 1994

Journal: :Archives of disease in childhood 2003
F Rusconi C Panisi R M Dellepiane F Cardinale L Chini B Martire N Bonelli G Felisati M C Pietrogrande

AIMS To prospectively evaluate sinopulmonary disease in 24 patients with primary humoral immunodeficiency (11 with agammaglobulinaemia, nine with isolated IgA deficiency, and two with common variable immunodeficiency) and chronic productive cough, ascertain the usefulness of chest high resolution computed tomography (HRCT) in evaluating the progression of lung disease, and test a therapeutic ap...

2013
HONGGANG WANG MIN WANG ZHINING FAN GUOZHONG JI FAMING ZHANG

Primary immunodeficiency is a disease characterized by reduced levels of serum immunoglobulins and multiple clinical manifestations. Patients with primary immunodeficiency frequently present with gastrointestinal symptoms, such as diarrhea, malabsorption and weight loss. The mainstay of treatment is replacement therapy with intravenous immunoglobulin (IVIG). In the current study, we report the ...

Journal: :Human Molecular Genetics 2019

Journal: :American Journal of Roentgenology 1975

Journal: :iranian journal of allergy, asthma and immunology 0
nasser ebrahimi daryani asghar aghamohammadi mohammad-reza mousavi mirkala mohammad bashashati nima rezaei babak haghpanah

common variable immunodeficiency (cvid) is a primary immunodeficiency disease characterized by hypogammaglobulinemia and recurrent bacterial infections especially in respiratory and gastrointestinal systems. we present here 2 cases of cvid with gastrointestinal complications. case 1 is a 25-year-old man with a history of chronic diarrhoea from childhood. ultrasonography revealed ascites, with l...

2017
Maria Francisca Moraes-Fontes Amy P Hsu Iris Caramalho Catarina Martins Ana Carolina Araújo Filipa Lourenço Anna V Taulaigo Ana Lladó Steven M Holland Gulbu Uzel

Primary immunodeficiency disorders are rarely diagnosed in adults but must be considered in the differential diagnosis of combined recurrent infections and autoimmune disease. We describe a patient with CTLA-4 haploinsufficiency and an abnormal regulatory T-cell phenotype. Unusually, infections were more severe than autoimmunity, illustrating therapeutic challenges in disease course.

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