A clinical criterion to exclude the hyperimmunoglobulin D syndrome (mild mevalonate kinase deficiency) in patients with recurrent fever

Journal of Rheumatology

Volumn 36, Issue 8, 2009, Pages 1677-1681

  Steichen, Olivier ^a   Van Der Hilst, Jeroen ^b   Simon, Anna ^b   Cuisset, Laurence ^c   Grateau, Gilles ^a  

^a HÔPITAL TENON   (France)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^c Cochin Hospital ^*  (France)

Author keywords

Clinical prediction rule; Fever; Genetic screening; Mevalonate kinase deficiency; Sensitivity and specificity

Indexed keywords

IMMUNOGLOBULIN D; MEVALONATE KINASE;

ABDOMINAL PAIN; ADOLESCENT; ADULT; ARTHRALGIA; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHILD; CLINICAL FEATURE; CLINICAL LABORATORY; CONFIDENCE INTERVAL; DIAGNOSTIC ACCURACY; DIARRHEA; DISEASE DURATION; FEMALE; FRANCE; GENE MUTATION; GENETIC SCREENING; HEPATOSPLENOMEGALY; HUMAN; HYPERIMMUNOGLOBULINEMIA D AND PERIODIC FEVER SYNDROME; INFLAMMATORY DISEASE; LYMPHADENOPATHY; MAJOR CLINICAL STUDY; MALE; NETHERLANDS; ONSET AGE; PREDICTION; PRIORITY JOURNAL; RASH; RECURRENT FEVER; VALIDATION STUDY; VOMITING;

ADOLESCENT; ADULT; AGE OF ONSET; ALGORITHMS; CHILD; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; FEMALE; FEVER OF UNKNOWN ORIGIN; GENETIC SCREENING; HUMANS; JOB'S SYNDROME; MALE; MEVALONATE KINASE DEFICIENCY; PAIN; UNNECESSARY PROCEDURES; YOUNG ADULT;

EID: 68849116499     PISSN: 0315162X     EISSN: None     Source Type: Journal    
DOI: 10.3899/jrheum.081313     Document Type: Article

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