Literature DB >> 9894634

Hereditary fevers.

G Grateau1, J P Drenth, M Delpech.   

Abstract

Hereditary fevers are a group of rare disorders of the inflammatory response. Clinical features include recurrent attacks of fever and organ-localized inflammation. Minimal clinical variations, a unique biochemical-specific abnormality, and the mode of genetic inheritance distinguish the three main diseases: familial Mediterranean fever, hyperimmunoglobulinemia D and periodic fever syndrome, and autosomal dominant recurrent fever. The complete elucidation of pathogenesis of these intriguing disorders will be provided by the genetic studies currently in progress.

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Year:  1999        PMID: 9894634     DOI: 10.1097/00002281-199901000-00013

Source DB:  PubMed          Journal:  Curr Opin Rheumatol        ISSN: 1040-8711            Impact factor:   5.006


  3 in total

1.  Genetic linkage of the Muckle-Wells syndrome to chromosome 1q44.

Authors:  L Cuisset; J P Drenth; J M Berthelot; A Meyrier; G Vaudour; R A Watts; D G Scott; A Nicholls; S Pavek; C Vasseur; J S Beckmann; M Delpech; G Grateau
Journal:  Am J Hum Genet       Date:  1999-10       Impact factor: 11.025

2.  Where has secondary amyloid gone?

Authors:  B P Hazenberg; M H van Rijswijk
Journal:  Ann Rheum Dis       Date:  2000-08       Impact factor: 19.103

3.  Identification of a locus on chromosome 1q44 for familial cold urticaria.

Authors:  H M Hoffman; F A Wright; D H Broide; A A Wanderer; R D Kolodner
Journal:  Am J Hum Genet       Date:  2000-03-30       Impact factor: 11.025

  3 in total

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