Literature DB >> 12427362

Immunodeficiency and genetic conditions that cause arthritis in childhood.

Pierre Quartier1, Anne-Marie Prieur.   

Abstract

Many conditions can cause or be associated with arthritis in childhood. The authors of this paper will review the situations in which underlying immunodeficiency or defective regulation of lymphocyte homeostasis must be suspected, and discuss, for some of these diseases, the genetic bases and pathogenesis. In the second part of this article, the authors will focus on other diseases that can cause arthritis in childhood, often with other symptoms, and for which evidence of an association with genetic abnormalities has been recently discovered. Finally, the authors will discuss the implications of recent findings regarding the role of some genes as causing or modulating factors in juvenile idiopathic arthritis and related disorders, as well as observations made in adults and in animal models of inflammation and autoimmunity.

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Year:  2002        PMID: 12427362     DOI: 10.1007/s11926-002-0054-5

Source DB:  PubMed          Journal:  Curr Rheumatol Rep        ISSN: 1523-3774            Impact factor:   4.686


  57 in total

Review 1.  Cytokine polymorphisms and inflammation.

Authors:  P Woo
Journal:  Clin Exp Rheumatol       Date:  2000 Nov-Dec       Impact factor: 4.473

2.  Human immunodeficiency virus infection associated arthritis: clinical characteristics.

Authors:  A Berman; P Cahn; H Perez; A Spindler; E Lucero; S Paz; L R Espinoza
Journal:  J Rheumatol       Date:  1999-05       Impact factor: 4.666

3.  Enteroviral meningoencephalitis as a complication of X-linked hyper IgM syndrome.

Authors:  C K Cunningham; C A Bonville; H D Ochs; K Seyama; P A John; H A Rotbart; L B Weiner
Journal:  J Pediatr       Date:  1999-05       Impact factor: 4.406

4.  Hyper-IgM syndrome associated with rheumatoid arthritis: report of RA in a patient with primary impaired CD40 pathway.

Authors:  J Sibilia; A Durandy; T Schaeverbeke; J P Fermand
Journal:  Br J Rheumatol       Date:  1996-03

5.  CARD15 mutations in Blau syndrome.

Authors:  C Miceli-Richard; S Lesage; M Rybojad; A M Prieur; S Manouvrier-Hanu; R Häfner; M Chamaillard; H Zouali; G Thomas; J P Hugot
Journal:  Nat Genet       Date:  2001-09       Impact factor: 38.330

Review 6.  ATM: from gene to function.

Authors:  G Rotman; Y Shiloh
Journal:  Hum Mol Genet       Date:  1998       Impact factor: 6.150

Review 7.  Genetic, biochemical, and clinical features of chronic granulomatous disease.

Authors:  B H Segal; T L Leto; J I Gallin; H L Malech; S M Holland
Journal:  Medicine (Baltimore)       Date:  2000-05       Impact factor: 1.889

8.  C1q deficiency and autoimmunity: the effects of genetic background on disease expression.

Authors:  Daniel A Mitchell; Matthew C Pickering; Joanna Warren; Liliane Fossati-Jimack; Josefina Cortes-Hernandez; H Terence Cook; Marina Botto; Mark J Walport
Journal:  J Immunol       Date:  2002-03-01       Impact factor: 5.422

9.  Long-term itraconazole prophylaxis against Aspergillus infections in thirty-two patients with chronic granulomatous disease.

Authors:  R Mouy; F Veber; S Blanche; J Donadieu; R Brauner; J C Levron; C Griscelli; A Fischer
Journal:  J Pediatr       Date:  1994-12       Impact factor: 4.406

10.  The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM.

Authors:  J Sayos; C Wu; M Morra; N Wang; X Zhang; D Allen; S van Schaik; L Notarangelo; R Geha; M G Roncarolo; H Oettgen; J E De Vries; G Aversa; C Terhorst
Journal:  Nature       Date:  1998-10-01       Impact factor: 49.962

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