The clinical and laboratory spectrum of dedicator of cytokinesis 8 immunodeficiency syndrome in patients with a unique mutation

Immunologic Research

Volumn 65, Issue 3, 2017, Pages 651-657

  Broides, Arnon ^a,b   Mandola, Amarilla B ^a,b   Levy, Jacov ^a,b   Yerushalmi, Baruch ^a,b   Pinsk, Vered ^a,b   Eldan, Michal ^c   Shubinsky, George ^a,b   Hadad, Nurit ^a,b   Levy, Rachel ^a,b   Nahum, Amit ^a,b   Ben Harosh, Miriam ^a,b   Lev, Atar ^d   Simon, Amos ^d   Somech, Raz ^d  

^a BEN GURION UNIVERSITY OF THE NEGEV   (Israel)

^b BEN GURION UNIVERSITY OF THE NEGEV   (Israel)

^c CLALIT HEALTH SERVICES   (Israel)

^d TEL AVIV UNIVERSITY   (Israel)

Author keywords

Combined immunodeficiency; Genotype; IgE; Phenotype

Indexed keywords

IMMUNOGLOBULIN E; SERINE; DOCK8 PROTEIN, HUMAN; GUANINE NUCLEOTIDE EXCHANGE FACTOR;

ADOLESCENT; AGE DISTRIBUTION; ANTIPNEUMOCOCCAL ANTIBODY DEFICIENCY; ARTICLE; ASTHMA; AUTOIMMUNITY; BRONCHIECTASIS; CHILD; CLINICAL ARTICLE; CLINICAL EXAMINATION; DOCK8 GENE; ECZEMA; EPIGENETICS; FAMILY HISTORY; FAMILY STUDY; FOOD ALLERGY; GENE; GENOTYPE PHENOTYPE CORRELATION; HERPES SIMPLEX KERATITIS; HOMOZYGOSITY; HUMAN; HUMORAL IMMUNE DEFICIENCY; HYPER IGE SYNDROME; HYPEREOSINOPHILIC SYNDROME; IMMUNOGLOBULIN BLOOD LEVEL; INFANT; LABORATORY TEST; MALE; MALIGNANT NEOPLASM; MEDICAL RECORD REVIEW; MUTATIONAL ANALYSIS; PNEUMONIA; PRIORITY JOURNAL; RETROSPECTIVE STUDY; SIBLING; AGE; ARAB; BLOOD; CONSANGUINITY; GENETICS; GENOTYPE; IMMUNOLOGY; MUTATION; PEDIGREE; PHENOTYPE; PRESCHOOL CHILD; RECURRENT DISEASE; STREPTOCOCCUS PNEUMONIA; YOUNG ADULT;

ADOLESCENT; AGE FACTORS; ARABS; ASTHMA; BRONCHIECTASIS; CHILD; CHILD, PRESCHOOL; CONSANGUINITY; ECZEMA; GENOTYPE; GUANINE NUCLEOTIDE EXCHANGE FACTORS; HUMANS; IMMUNOGLOBULIN E; INFANT; JOB SYNDROME; MUTATION; PEDIGREE; PHENOTYPE; PNEUMONIA, PNEUMOCOCCAL; RECURRENCE; RETROSPECTIVE STUDIES; YOUNG ADULT;

EID: 85008627156     PISSN: 0257277X     EISSN: 15590755     Source Type: Journal    
DOI: 10.1007/s12026-016-8883-x     Document Type: Article

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