Global systematic review of primary immunodeficiency registries
Introduction During the last 4 decades, registration of patients with primary
immunodeficiencies (PID) has played an essential role in different aspects of these diseases …
immunodeficiencies (PID) has played an essential role in different aspects of these diseases …
Selective IgA deficiency: epidemiology, pathogenesis, clinical phenotype, diagnosis, prognosis and management
Selective immunoglobulin A deficiency (SI g AD) is the most common primary antibody
deficiency. Although more patients with SI g AD are asymptomatic, selected patients suffer …
deficiency. Although more patients with SI g AD are asymptomatic, selected patients suffer …
Are complement deficiencies really rare? Overview on prevalence, clinical importance and modern diagnostic approach
AS Grumach, M Kirschfink - Molecular immunology, 2014 - Elsevier
Complement deficiencies comprise between 1 and 10% of all primary immunodeficiencies
(PIDs) according to national and supranational registries. They are still considered rare and …
(PIDs) according to national and supranational registries. They are still considered rare and …
[HTML][HTML] Clinical implications of systematic phenotyping and exome sequencing in patients with primary antibody deficiency
H Abolhassani, A Aghamohammadi, M Fang… - Genetics in …, 2019 - Elsevier
Purpose The etiology of 80% of patients with primary antibody deficiency (PAD), the second
most common type of human immune system disorder after human immunodeficiency virus …
most common type of human immune system disorder after human immunodeficiency virus …
The hyper IgM syndromes: Epidemiology, pathogenesis, clinical manifestations, diagnosis and management
Abstract Hyper Immunoglobulin M syndrome (HIGM) is a rare primary immunodeficiency
disorder characterized by low or absent levels of serum IgG, IgA, IgE and normal or …
disorder characterized by low or absent levels of serum IgG, IgA, IgE and normal or …
Fourth update on the Iranian National Registry of Primary Immunodeficiencies: integration of molecular diagnosis
H Abolhassani, F Kiaee, M Tavakol… - Journal of clinical …, 2018 - Springer
Background The number of inherited diseases and the spectrum of clinical manifestations of
primary immunodeficiency disorders (PIDs) are ever-expanding. Molecular diagnosis using …
primary immunodeficiency disorders (PIDs) are ever-expanding. Molecular diagnosis using …
Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency
Background Combined immunodeficiencies (CIDs) are diseases of defective adaptive
immunity with diverse clinical phenotypes. Although CIDs are more prevalent in the Middle …
immunity with diverse clinical phenotypes. Although CIDs are more prevalent in the Middle …
Infectious and noninfectious pulmonary complications in patients with primary immunodeficiency disorders.
Primary immunodeficiency disorders (PIDs) are caused by 1 or more defects of the immune
system. Patients are more likely to experience recurrent and/or severe infections and tend to …
system. Patients are more likely to experience recurrent and/or severe infections and tend to …
[HTML][HTML] Primary immunodeficiency diseases in highly consanguineous populations from Middle East and North Africa: epidemiology, diagnosis, and care
H Al-Mousa, B Al-Saud - Frontiers in immunology, 2017 - frontiersin.org
Middle East and North Africa region (MENA) 1 populations are of different ethnic origins.
Consanguineous marriages are common practice with an overall incidence ranging …
Consanguineous marriages are common practice with an overall incidence ranging …
Clinical, immunologic, molecular analyses and outcomes of iranian patients with LRBA deficiency: a longitudinal study
Background LPS‐responsive beige‐like anchor protein (LRBA) deficiency is a combined
immunodeficiency caused by mutation in LRBA gene. The patients have a variety of clinical …
immunodeficiency caused by mutation in LRBA gene. The patients have a variety of clinical …