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Volumn 159, Issue 1, 2015, Pages 58-62
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A case of XMEN syndrome presented with severe auto-immune disorders mimicking autoimmune lymphoproliferative disease
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Author keywords
[No Author keywords available]
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Indexed keywords
CD19 ANTIGEN;
CD3 ANTIGEN;
CD4 ANTIGEN;
CD8 ANTIGEN;
FAS LIGAND;
FC RECEPTOR;
GAMMA INTERFERON;
GANCICLOVIR;
HEMOGLOBIN;
IMMUNOGLOBULIN;
IMMUNOGLOBULIN A;
IMMUNOGLOBULIN E;
IMMUNOGLOBULIN G;
IMMUNOGLOBULIN M;
INTERLEUKIN 10;
INTERLEUKIN 18;
MAGNESIUM;
TUMOR NECROSIS FACTOR;
CATION TRANSPORT PROTEIN;
MAGT1 PROTEIN, HUMAN;
ADOLESCENT;
ALLOGENEIC HEMATOPOIETIC STEM CELL TRANSPLANTATION;
ANEMIA;
AUTOIMMUNE DISEASE;
AUTOIMMUNE HEPATITIS;
BRONCHITIS;
CASE REPORT;
CLINICAL FEATURE;
COMBINED IMMUNODEFICIENCY;
COMPUTER ASSISTED TOMOGRAPHY;
CONTROLLED STUDY;
CONVALESCENCE;
CYTOKINE PRODUCTION;
CYTOMEGALOVIRUS INFECTION;
DIET SUPPLEMENTATION;
ELECTROMYOGRAPHY;
EXON;
FLU LIKE SYNDROME;
FOLLOW UP;
FRAMESHIFT MUTATION;
GENE;
GENE DUPLICATION;
GENE MUTATION;
GENETIC ANALYSIS;
GRANULOCYTE;
GUILLAIN BARRE SYNDROME;
HEMIZYGOSITY;
HEMOGLOBIN BLOOD LEVEL;
HODGKIN DISEASE;
HOSPITAL ADMISSION;
HUMAN;
HUMAN TISSUE;
IMMUNE DEFICIENCY;
K562 CELL LINE;
LETTER;
LEUKOCYTE COUNT;
LIVER BIOPSY;
LIVER FUNCTION TEST;
LYMPH NODE BIOPSY;
LYMPHADENOPATHY;
LYMPHOCYTE COUNT;
LYMPHOCYTOPENIA;
LYMPHOPROLIFERATIVE DISEASE;
MAGT1 GENE;
MALE;
MAST CELL DEGRANULATION;
MEDIASTINUM LYMPH NODE;
MUSCLE WEAKNESS;
NATURAL KILLER CELL;
NEUROLOGIST;
NEUTROPHIL COUNT;
NUCLEAR MAGNETIC RESONANCE IMAGING;
OPHTHALMOPLEGIA;
PHENOTYPE;
PHYSIOTHERAPY;
PLASMAPHERESIS;
PRIORITY JOURNAL;
PROTEIN CONTENT;
SEQUENCE ANALYSIS;
SEROLOGY;
SINUSITIS;
SPLENECTOMY;
STEROID THERAPY;
THROMBOCYTOPENIA;
ULTRASOUND;
UPPER RESPIRATORY TRACT INFECTION;
WALKING DIFFICULTY;
X CHROMOSOME LINKED DISORDER;
XMEN SYNDROME;
AUTOIMMUNE DISEASES;
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME;
DIFFERENTIAL DIAGNOSIS;
EPSTEIN-BARR VIRUS INFECTIONS;
GENETICS;
MUTATION;
NEOPLASMS;
SYNDROME;
X-LINKED COMBINED IMMUNODEFICIENCY DISEASES;
ADOLESCENT;
AUTOIMMUNE DISEASES;
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME;
CATION TRANSPORT PROTEINS;
DIAGNOSIS, DIFFERENTIAL;
EPSTEIN-BARR VIRUS INFECTIONS;
HODGKIN DISEASE;
HUMANS;
MALE;
MUTATION;
NEOPLASMS;
SYNDROME;
X-LINKED COMBINED IMMUNODEFICIENCY DISEASES;
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EID: 84929463191
PISSN: 15216616
EISSN: 15217035
Source Type: Journal
DOI: 10.1016/j.clim.2015.04.015 Document Type: Letter |
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Times cited : (38)
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References (7)
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