Results 31 to 40 of about 4,530 (166)

Common variable immunodeficiency – case report

open access: yesJournal of Health Sciences, 2013
Common variable immunodeficiency (CVID) or acquired hypogammaglobulinemia is the type of primary immunodeficiency. Deregulation of the immune system, leading to hypogammaglobulinemia, defective activation and proliferation of T cells and dendritic cells,
Emina Vukas   +3 more
doaj   +3 more sources

Management of a patient with common variable immunodeficiency and hepatopathy

open access: yesAllergy, Asthma & Clinical Immunology, 2023
Background Common variable Immunodeficiency (CVID) is a primary immunodeficiency disorder and the most common form of severe antibody deficiency. Both children and adults are affected and clinical manifestations vary widely.
Lea Grümme, Hendrik Schulze-Koops
doaj   +1 more source

Chronic tubulo-interstitial nephritis in common variable immunodeficiency: A rare association

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2014
Common variable immunodeficiency (CVID) is characterized by reduced serum immunoglobulin levels and repeated serious bacterial infections involving different organ systems. Chronic kidney disease (CKD) is an uncommon association with CVID. Chronic tubulo-
Sumantra Sarkar   +3 more
doaj   +1 more source

Common variable immunodeficiency in an 11-year-old girl – a case report

open access: yesJournal of Pre-Clinical and Clinical Research, 2020
Common variable immunodeficiency (CVID) is one of the most prevalent, heterogenous primary immunodeficiency syndromes in children and adults. Besides impaired immunoglobulin production by B cells, abnormalities in almost all components of the immune ...
Joanna Pawłowska   +2 more
doaj   +1 more source

Common variable immunodeficiency associated enteropathy: a diagnostic enigma in developing countries

open access: yesJournal of the Pakistan Medical Association
Common variable immunodeficiency (CVID) is the most prevalent primary immunodeficiency disorder with different phenotypes and aetiologies. It is characterised by hypogammaglobulinaemia, defects in specific antibody response, erroneous activation and ...
Muhammad Aftab Hassan   +4 more
doaj   +1 more source

Characterization of infectious and non-infectious gastrointestinal disease in common variable immunodeficiency: analysis of 114 patient cohort

open access: yesFrontiers in Immunology, 2023
Common Variable Immunodeficiency (CVID), a complex primary immunodeficiency syndrome defined by defective B cell responses to infection and vaccination, has heterogeneous clinical manifestations.
David A. Sanchez   +4 more
doaj   +1 more source

Common Variable Immunodeficiency (CVID): A Case Report

open access: yesInternal Medicine and Medical Investigation Journal, 2017
Common variable immune deficiency disease is the most prevalent acquired immune deficiency in human being after selective immunoglobulin A deficiency. It causes reduction of immunoglobulin levels and specific antibodies production and enhancement of recurrent and chronic infections risk, especially respiratory infections.
Maryam Montazeri   +3 more
openaire   +1 more source

The safe and effective use of tofacitinib and ustekinumab combination therapy in infantile onset inflammatory bowel disease

open access: yesJPGN Reports, EarlyView.
Abstract Infantile‐onset inflammatory bowel disease (IOIBD) is a rare and severe subset of very‐early‐onset IBD, often associated with immune dysregulation and poor response to conventional therapies. Data regarding the use of Janus kinase inhibitors (JAKI) in this population is limited.
Smridhi Mahajan   +2 more
wiley   +1 more source

Refractory Eczema as a Presenting Feature of Common Variable Immunodeficiency

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Common variable immunodeficiency (CVID) is the most prevalent symptomatic inborn error of immunity (IEI) in adults. It presents with recurrent infections and non‐infectious complications, including autoimmunity, lymphoproliferation and dermatitis.
Mercedes Sanchez‐Diaz   +2 more
wiley   +1 more source

Phenotype‐specific immune profiles and outcomes in childhood autoimmune neutropenia: A 20‐year cohort study

open access: yesBritish Journal of Haematology, EarlyView.
Summary Childhood autoimmune neutropenia (AIN) encompasses heterogeneous entities; phenotype‐specific immunological profiles and their relationship to infection outcomes remain incompletely defined. To characterise clinical, immunological and long‐term outcomes across distinct phenotypes of childhood AIN.
Ioanna Saougou   +5 more
wiley   +1 more source

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