Major histocompatibility complex class II expression deficiency is an autosomal recessive primary combined immunodeficiency. The prevalence of this deficiency is the highest in Mediterranean areas, especially North Africa. Early diagnosis is essential due to high mortality in the first 2 years of life. Prognosis is very poor when bone marrow transplantation cannot be performed. We report the case of an infant with major histocompatibility complex class II expression deficiency revealed by hypoxemic bronchiolitis due to Pneumocystis jiroveci
Abstract BACKGROUND: MHC class II deficiency leads to defective CD4+ T-cell function that results f...
Chronic granulomatous disease is a diverse group of hereditary diseases characterized by neutrophils...
Background: Wheezing, starting early in life, is a heterogeneous medical condition caused by airway ...
Copyright © 2013 S. Hammami et al. This is an open access article distributed under the Creative Com...
Major histocompatibility complex (MHC) class II deficiency is a rare autosomal recessive form of pri...
The class II major histocompatibility complex antigen deficiency syndrome is a rare immunodeficiency...
PurposeMajor histocompatibility complex class II (MHC-II) deficiency is a rare inborn error of immun...
The MHC II deficiency is a rare autosomal recessive primary immunodeficiency syndrome with increased...
The MHC II deficiency is a rare autosomal recessive primary immunodeficiency syndrome with increase...
A 4-year-old boy with hypochondroplasia was admitted to our clinic with complaints of bronchopneumon...
LPS-Responsive Beige-like Anchor (LRBA) deficiency is a disease which has recently been described in...
A 6-week-old boy presented to our hospital with upper respiratory tract infection and severe anemia ...
SummaryObliterative bronchiolitis (OB) is known to result from many causes, such as post-bone marrow...
Chronic granulomatous disease (CGD) is a primary immune deficiency disorder of the phagocytes. In th...
Patients with primary immunodeficiencies are usually susceptible to enterovirus infections and have ...
Abstract BACKGROUND: MHC class II deficiency leads to defective CD4+ T-cell function that results f...
Chronic granulomatous disease is a diverse group of hereditary diseases characterized by neutrophils...
Background: Wheezing, starting early in life, is a heterogeneous medical condition caused by airway ...
Copyright © 2013 S. Hammami et al. This is an open access article distributed under the Creative Com...
Major histocompatibility complex (MHC) class II deficiency is a rare autosomal recessive form of pri...
The class II major histocompatibility complex antigen deficiency syndrome is a rare immunodeficiency...
PurposeMajor histocompatibility complex class II (MHC-II) deficiency is a rare inborn error of immun...
The MHC II deficiency is a rare autosomal recessive primary immunodeficiency syndrome with increased...
The MHC II deficiency is a rare autosomal recessive primary immunodeficiency syndrome with increase...
A 4-year-old boy with hypochondroplasia was admitted to our clinic with complaints of bronchopneumon...
LPS-Responsive Beige-like Anchor (LRBA) deficiency is a disease which has recently been described in...
A 6-week-old boy presented to our hospital with upper respiratory tract infection and severe anemia ...
SummaryObliterative bronchiolitis (OB) is known to result from many causes, such as post-bone marrow...
Chronic granulomatous disease (CGD) is a primary immune deficiency disorder of the phagocytes. In th...
Patients with primary immunodeficiencies are usually susceptible to enterovirus infections and have ...
Abstract BACKGROUND: MHC class II deficiency leads to defective CD4+ T-cell function that results f...
Chronic granulomatous disease is a diverse group of hereditary diseases characterized by neutrophils...
Background: Wheezing, starting early in life, is a heterogeneous medical condition caused by airway ...