Common variable immunodeficiency: Familial inheritance and autoimmune manifestations in two siblings

Turkish Journal of Pediatrics

Volumn 52, Issue 1, 2010, Pages 89-93

  Edeer Karaca, Neslihan ^a   Gülez, Nesrin ^a   Aksu, Güzide ^a   Kütükçüler, Necil ^a  

^a EGE UNIVERSITY SCHOOL OF MEDICINE   (Turkey)

Author keywords

Autoimmunity; Common variable immunodeficiency; Familial inheritance

Indexed keywords

ANTIBIOTIC AGENT; ANTINUCLEAR ANTIBODY; CD19 ANTIGEN; CD3 ANTIGEN; CD8 ANTIGEN; CORTICOSTEROID; IMMUNOGLOBULIN; IMMUNOGLOBULIN A; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M; MESALAZINE; METHOTREXATE; NONSTEROID ANTIINFLAMMATORY AGENT; PREDNISOLONE; SALAZOSULFAPYRIDINE;

ANEMIA; ARTHRALGIA; ARTICLE; AUTOIMMUNITY; CASE REPORT; CHILD; COLONOSCOPY; COMMON VARIABLE IMMUNODEFICIENCY; DIARRHEA; DRUG DOSE REDUCTION; ECHOGRAPHY; ENTERITIS; EXTERNAL EAR; FAMILIAL DISEASE; HUMAN; IMMUNOGLOBULIN BLOOD LEVEL; IMMUNOGLOBULIN DEFICIENCY; INHERITANCE; JOINT EFFUSION; JUVENILE RHEUMATOID ARTHRITIS; KNEE PAIN; LABORATORY TEST; LOW DRUG DOSE; LYMPHOCYTE SUBPOPULATION; MALE; METACARPOPHALANGEAL JOINT; NAUSEA AND VOMITING; PNEUMONIA; PRESCHOOL CHILD; RECURRENT INFECTION; RELAPSING POLYCHONDRITIS; RESPIRATORY FAILURE; RESPIRATORY TRACT INFECTION; SIBLING; SKIN INFLAMMATION; SWELLING; THROMBOCYTOSIS; WRIST;

CHILD, PRESCHOOL; COMMON VARIABLE IMMUNODEFICIENCY; FATAL OUTCOME; HUMANS; IMMUNOGLOBULINS, INTRAVENOUS; INFANT;

EID: 77950424916     PISSN: 00414301     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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