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COMMON VARIABLE IMMUNODEFICIENCY [PDF]

National Journal of Medical Research, 2013
  Common variable immunodeficiency (CVID) is a form of severe antibody deficiency with an estimated prevalence of 1 in 25,000 to 1 in 100,000. The disorder apparently results from currently undefined immune deregulations resulting in failed B-cell ...
Hardik Parmar, K M Mehariya, Charul Purani   +2 more
doaj   +8 more sources

Common immunodeficiency variable in adults

Revista Alergia México, 2017
Primary immunodeficiencies (PIDs) are low-incidence diseases caused by defects in genes involved in the development, maintenance, and regulation of the immune system. Common variable immunodeficiency (CVID) is the most common symptomatic immunodeficiency
Patricia María O’Farrill-Romanillos, Diana Andrea Herrera-Sánchez, Cecilia Hernández-Fernández, Eunice Giselle López-Rocha   +3 more
doaj   +4 more sources

Common variable immunodeficiency in adults [PDF]

Терапевтический архив, 2016
The paper analyzes 7 cases of common variable immune deficiency (CVID), a primary immunodeficiency disease. All the cases were detected in outpatients over the age of 40 years.
N V Shabashova, L V Filippova, A E Uchevatkina, E V Frolova   +3 more
doaj   +3 more sources

Common variable immunodeficiency

Medicina Clínica (English Edition)
Common variable immunodeficiency (CVID) is characterized by defective differentiation of B lymphocytes, hypogammaglobulinemia, and infections, although its clinical presentation is much more heterogeneous, with autoimmunity, interstitial lung disease, enteropathy, lymphoproliferation, malignancy, among others.
Solanich, Xavier, Antoli, Arnau, Alsina, Laia   +2 more
europepmc   +8 more sources

Common variable immunodeficiency in a patient with Noonan syndrome

Alergologia Polska
Noonan syndrome is a disease that occurs in 1 in 1,000–2,500 live births, mostly inherited in an autosomal dominant manner. Noonan syndrome is a clinically and genetically heterogeneous disease that may be accompanied by growth retardation, prominent ...
Öner Özdemir, Ümmügülsüm Dikici, Ece Tüsüz Önata, Recep Polat   +3 more
doaj   +2 more sources

Common variable immunodeficiency disorder: a clinical case [PDF]

Медицинская иммунология, 2021
Primary immunodeficiency is a rare congenital pathology associated with failure of immune system, manifested by disturbances of its functions. These defects lead to increased susceptibility of patients to various infectious agents, as well as the ...
E. A. Sobko, I. V. Demko, I. A. Soloveva, A. Yu. Kraposhina, N. V. Gordeeva, D. A. Anikin, N. S. Pronkina, O. P. Ischenko   +7 more
doaj   +2 more sources

Autoimmune cytopenias related to common variable immunodeficiency

Zdravniški Vestnik, 2011
Background: Common variable immunodeficiency disorders are characterised by defective antibody production leading to recurrent infections. Noninfective complications are a consequence of autoimmunity, granuloma and polyclonal lymphoid infiltration.
Vlasta Petric, Romana Rotdajč, Maja Šeruga   +2 more
doaj   +1 more source

Genetics and clinical phenotypes in common variable immunodeficiency

Frontiers in Genetics
Common variable immunodeficiency (CVID) is one of the most common symptomatic groups of inborn errors of immunity. In addition to infections resulting from insufficient levels of immune globulins and antibodies, many patients develop inflammatory or ...
Bertrand Boisson, Jean-Laurent Casanova, Charlotte Cunningham-Rundles   +2 more
exaly   +3 more sources

Common Variable Immunodeficiency [PDF]

Clinical Reviews in Allergy & Immunology, 2000
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Strober, Warren, Chua, Kevin
openaire   +4 more sources

Polyautoimmunity Reflecting Immune Dysregulation in Common Variable Immunodeficiency [PDF]

Biomedicines
Background: Common variable immunodeficiency (CVID) is the most frequent symptomatic inborn error of immunity (IEI) in adulthood. Other than recurrent infections, CVID may present with non-infectious complications such as enteropathy, lymphoproliferation,
Maria Giovanna Danieli, Giuseppe Murdaca, Cristina Mezzanotte, Ilaria Claudi, Elena Buti, Matteo Martini, Maria Beatrice Bilò, Sebastiano Gangemi, Gianluca Moroncini   +8 more
doaj   +2 more sources