نتایج جستجو برای: common variable immunodeficiency cvid

تعداد نتایج: 1013055  

2015
Tatiane Pavan-Ramos Ana Paula Willy-Fabro Ana Carolina Rozalem Juliana T Lessa Mazzucchelli Beatriz Costa Carvalho

Background Common Variable Immunodeficiency (CVID) is characterized by reduced serum levels of immunoglobulins (Ig) and its treatment requires regular infusion of intravenous immunoglobulin (IVIG). Eventually CVID female patients will reach reproductive age and it is known that maternofetal transplacental transport of antibodies is important to protect the child in the first months of life. The...

2012
Kenji Tsuji Haruhito Adam Uchida Tetsuichirou Ono Tatsuyuki Inoue Katsuji Shinagawa Shinji Kitamura Yohei Maeshima Hitoshi Sugiyama Hirofumi Makino

BACKGROUND Common variable immunodeficiency (CVID) is a disorder characterized by hypogammaglobulinemia without a known predisposing cause. CASE PRESENTATION We report a 36-year-old man who had suffered membranoproliferative glomerulonephritis (MPGN) in his childhood, later diagnosed with CVID at 35 years of age. He presented at our hospital with signs of proteinuria. A renal biopsy revealed ...

Journal: :Journal of autoimmunity 2011
Julien Boileau Gael Mouillot Laurence Gérard Maryvonnick Carmagnat Claire Rabian Eric Oksenhendler Jean-Louis Pasquali Anne-Sophie Korganow

Common variable immunodeficiency (CVID) is the most frequent clinically expressed primary immunodeficiency in adults and is characterized by primary defective immunoglobulin production. Besides recurrent infectious manifestations, up to 20% of CVID patients develop autoimmune complications. In this study, we took advantages of the French DEFI database to investigate possible correlations betwee...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1998
T A Yousry M Strupp R Brüning

A patient is reported on with a common variable immunodeficiency syndrome (CVID), in whom chronic gastritis with antibodies against parietal cells and a cytomegalovirus associated enteritis led to vitamin B12 deficiency with consecutive subacute combined degeneration of the spinal cord. The resulting medullary changes, most probably representing demyelination, were visualised with MRI. The effe...

Journal: :Haematologica 2006
Maria Francesca Campagnoli Letizia Garbarini Paola Quarello Emanuela Garelli Adriana Carando Valentina Baravalle Alessandra Doria Alessandra Biava Annalisa Chiocchetti Angelo Rosolen Carlo Dufour Umberto Dianzani Ugo Ramenghi

Autoimmune lymphoproliferative disorders, including autoimmune lymphoproliferative syndrome (ALPS) and Dianzani autoimmune lymphoproliferative disease (DALD), are inherited defects of the Fas apoptotic pathway characterized by lymphoid accumulation and autoimmune manifestations. We report the molecular, clinical, immunologic features and the long-term progress of 31 patients. Four carried Fas g...

2015
Maira Pedreschi Marques Baldassin Anete Grumach Ana Karolina Barreto De Oliveira Jorge Kalil

Background Common Variable Immunodeficiency (CVID) is characterized by hypogammaglobulinaemia and impaired specific antibody production, resulting in increased susceptibility to infections, mainly of the respiratory tract. In an attempt to minimize the recurrent episodes of infections, some studies have recommended immunization with inactivated pathogens or subunits, however, experience with va...

2015
Andrés Felipe Zea-Vera Olga Lucia Agudelo-Rojas

Primary immunodeficiencies (PID) are traditionally considered childhood diseases; however, adults account for 35% of all patients with PID. Antibody deficiencies, especially Common Variable Immunodeficiency (CVID), which have their peak incidence in adulthood, require a high suspicion index. Even though the estimated frequency of CVID is not high (1:25,000), high rates of under diagnosis and un...

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...

Journal: :iranian journal of immunology 0
mohamed osama hegazi department of medicine ramesh kumar department of hematology, al adan hospital, kuwait mubarak alajmi department of medicine eman ibrahim department of hematology, al adan hospital, kuwait

0

Journal: :Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2015
Marion Malphettes Laurence Gérard Lionel Galicier David Boutboul Bouchra Asli Raphael Szalat Antoinette Perlat Agathe Masseau Nicolas Schleinitz Guillaume Le Guenno Jean-François Viallard Bernard Bonnotte Marie-Françoise Thiercelin-Legrand Laurence Sanhes Raphael Borie Sophie Georgin-Lavialle Claire Fieschi Eric Oksenhendler

BACKGROUND Good syndrome (GS) is a rare condition in which thymoma is associated with hypogammaglobulinemia. It is characterized by increased susceptibility to bacterial, viral, and fungal infections, as well as autoimmunity. Most patients have no circulating B cells. METHODS The French DEFicit Immunitaire de l'adulte cohort provides detailed clinical and immunological descriptions of 690 adu...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید