X-linked hyper-immunoglobulin M syndrome: Molecular genetic study and long-time follow-up of three generations of a Chinese family

International Archives of Allergy and Immunology

Volumn 140, Issue 1, 2006, Pages 1-8

  Lin, Sheng Chieh ^a,c   Shyur, Shyh Dar ^a   Lee, Wen I ^b   Ma, Yi Chun ^a   Huang, Li Hsin ^a  

^a MACKAY MEMORIAL HOSPITAL   (Taiwan)

^b CHANG GUNG CHILDREN S HOSPITAL   (Taiwan)

^c SAINT PAUL S HOSPITAL   (Taiwan)

Author keywords

CD40 ligand gene; Intravenous immunoglobulin therapy; X linked hyper immunoglobulin M syndrome

Indexed keywords

ASPARAGINE; CD4 ANTIGEN; CD40 LIGAND; IMMUNOGLOBULIN; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M; TUMOR NECROSIS FACTOR; TYROSINE;

ADULT; ANTIGEN EXPRESSION; BRONCHIECTASIS; CAUSE OF DEATH; CHINESE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; EXON; FAMILIAL DISEASE; FEMALE; FOLLOW UP; GENETIC ANALYSIS; HETEROZYGOTE; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPERIMMUNOGLOBULINEMIA M; IMMUNE DEFICIENCY; IMMUNOGLOBULIN BLOOD LEVEL; IMMUNOTHERAPY; INFANT; LABORATORY TEST; LONG TERM CARE; LYMPHOCYTE ACTIVATION; LYMPHOMA; MALE; MEDICAL RECORD REVIEW; MOLECULAR GENETICS; MUTAGENESIS; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; PROTEIN DOMAIN; REVIEW; SCLEROSING CHOLANGITIS; T LYMPHOCYTE; TREATMENT DURATION; X CHROMOSOME LINKED DISORDER;

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; ASIAN CONTINENTAL ANCESTRY GROUP; CD40 LIGAND; CHILD; CHILD, PRESCHOOL; COMMON VARIABLE IMMUNODEFICIENCY; DNA MUTATIONAL ANALYSIS; FEMALE; FOLLOW-UP STUDIES; GENETIC DISEASES, X-LINKED; HETEROZYGOTE DETECTION; HUMANS; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M; INFANT; MALE; PEDIGREE; SYNDROME;

EID: 33646015678     PISSN: 10182438     EISSN: None     Source Type: Journal    
DOI: 10.1159/000091744     Document Type: Review

References (24)

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