Hereditary recurrent fevers other than familial mediterranean fever;Fièvres intermittentes héréditaires, autres que la fièvre méditerranéenne familiale

Revue du Praticien

Volumn 52, Issue 2, 2002, Pages 155-159

  Grateau, Gilles ^a   Cuisset, Laurence ^a   Dodé, Catherine ^a   Delpech, Marc ^a  

^a HÔpital Cochin   (France)

Author keywords

[No Author keywords available]

Indexed keywords

TUMOR NECROSIS FACTOR RECEPTOR;

FAMILIAL DISEASE; FAMILIAL MEDITERRANEAN FEVER; FEVER; HYPERIMMUNOGLOBULINEMIA; INFLAMMATION; METABOLIC DISORDER; MUCKLE WELLS SYNDROME; RECURRENT DISEASE; REVIEW;

DIAGNOSIS, DIFFERENTIAL; FEVER; HUMANS; IMMUNOGLOBULIN D; INFLAMMATION; PERIODICITY; PROGNOSIS; RECEPTORS, TUMOR NECROSIS FACTOR; SYNDROME;

EID: 0037081150     PISSN: 00352640     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (18)

1. Genetically determined recurrent fevers
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3. A novel missense mutation (C30S) in the gene encoding tumor necrosis factor receptor I linked to autosomal-dominant recurrent fever with localized myositis in a French family
4. Tumor necrosis factor receptor-associated periodic syndrome: A novel syndrome with cutaneous manifestations
5. Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR I, define a family of dominantly inherited autoinflammatory syndromes
6. The tumor-necrosis-factor receptor-associated periodic syndrome: New mutations in TNFRSF la, ancestral origins, genotype-phenotype studies, and evidence for further genetic heterogeneity of periodic fevers
7. Hyperimmunoglobulinaemia D and periodic fever: A new syndrome
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11. Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome
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13. Molecular cloning of human mevalonate kinase and identification of a missense mutation in the genetic disease mevalonic aciduria
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16. Fièvre méditerranéenne familiale et syndrome de Muckle-Wells
17. Genetic linkage of the Muckle-Wells syndrome to chromosome iq44
18. Mutation of a new gene encoching a putative pyrin-like protein causes familial cold auto inflammatory syndrome and Muckle-Wells syndrome