Tendonitis in variant hyperimmunoglobulinaemia D and periodic fever syndrome - A rare disease with a new symptom

European Journal of Pediatrics

Volumn 164, Issue 6, 2005, Pages 391-394

  Armbrust, Sven ^a   Drenth, Joost P H ^d   Schröder, Carmen ^a   Domning, Ester ^c   Poeschl, Ernestine ^b   Wiersbitzky, Siegfried K W ^a  

^a University Children's Hospital   (Germany)

^b UNIVERSITY OF GREIFSWALD   (Germany)

^c General Hospital   (Germany)

^d RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Chromosome 12q24; HMG CoA reductase inhibitors; Hyperimmunoglobulinaemia D syndrome; Mevalonate kinase gene; Tendomyositis

Indexed keywords

HYPERIMMUNE GLOBULIN; MEVALONATE KINASE;

ADOLESCENT; ANAMNESIS; ARTICLE; BLOOD PROTEIN DISORDER; CASE REPORT; CLINICAL FEATURE; DIAGNOSTIC APPROACH ROUTE; DIAGNOSTIC IMAGING; DIAGNOSTIC TEST; FEMALE; FEVER; GENETIC ANALYSIS; HUMAN; HYPERIMMUNOGLOBULINEMIA D AND PERIODIC FEVER SYNDROME; INFORMED CONSENT; LABORATORY TEST; MEDICAL EXAMINATION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SYMPTOM; TENDINITIS;

ADOLESCENT; DNA MUTATIONAL ANALYSIS; FAMILIAL MEDITERRANEAN FEVER; FEMALE; GERMANY; HUMANS; HYPERGAMMAGLOBULINEMIA; IMMUNOGLOBULIN D; ORBITAL DISEASES; PEDIGREE; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR); TENDINOPATHY;

EID: 20944451844     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00431-005-1652-9     Document Type: Article

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