Add to ORKGCopyright © 2013 S. Hammami et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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 highmortality in the first 2 years of life. Prognosis is very poor when bonemarrow transplantation cannot be performed.We report the case of an infant with major histocompatibility complex class II expression deficiency revealed by hypoxemic...
Congenital central hypoventilation syndrome (CCHS) is a rare disease that is characterized by failur...
Chronic granulomatous disease is a diverse group of hereditary diseases characterized by neutrophils...
The heterozygous PHOX2B gene mutation is related to congenital central hypoventilation syndrome (CCH...
Major histocompatibility complex class II expression deficiency is an autosomal recessive primary co...
Major histocompatibility complex (MHC) class II deficiency is a rare autosomal recessive form of pri...
PurposeMajor histocompatibility complex class II (MHC-II) deficiency is a rare inborn error of immun...
The class II major histocompatibility complex antigen deficiency syndrome is a rare immunodeficiency...
The MHC II deficiency is a rare autosomal recessive primary immunodeficiency syndrome with increase...
The MHC II deficiency is a rare autosomal recessive primary immunodeficiency syndrome with increased...
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...
Chronic granulomatous disease (CGD) is a primary immune deficiency disorder of the phagocytes. In th...
Introduction. - Innate or acquired immune deficiency may show respiratory manifestations,often chara...
Congenital central hypoventilation syndrome (CCHS) is a rare disease that is characterized by failur...
In this article, we report a case of a 6-year-old girl, initially diagnosed with myelodysplastic syn...
Congenital central hypoventilation syndrome (CCHS) is a rare disease that is characterized by failur...
Chronic granulomatous disease is a diverse group of hereditary diseases characterized by neutrophils...
The heterozygous PHOX2B gene mutation is related to congenital central hypoventilation syndrome (CCH...
Major histocompatibility complex class II expression deficiency is an autosomal recessive primary co...
Major histocompatibility complex (MHC) class II deficiency is a rare autosomal recessive form of pri...
PurposeMajor histocompatibility complex class II (MHC-II) deficiency is a rare inborn error of immun...
The class II major histocompatibility complex antigen deficiency syndrome is a rare immunodeficiency...
The MHC II deficiency is a rare autosomal recessive primary immunodeficiency syndrome with increase...
The MHC II deficiency is a rare autosomal recessive primary immunodeficiency syndrome with increased...
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...
Chronic granulomatous disease (CGD) is a primary immune deficiency disorder of the phagocytes. In th...
Introduction. - Innate or acquired immune deficiency may show respiratory manifestations,often chara...
Congenital central hypoventilation syndrome (CCHS) is a rare disease that is characterized by failur...
In this article, we report a case of a 6-year-old girl, initially diagnosed with myelodysplastic syn...
Congenital central hypoventilation syndrome (CCHS) is a rare disease that is characterized by failur...
Chronic granulomatous disease is a diverse group of hereditary diseases characterized by neutrophils...
The heterozygous PHOX2B gene mutation is related to congenital central hypoventilation syndrome (CCH...