Clinical Rheumatology

, Volume 19, Issue 4, pp 262–264 | Cite as

A First Molecular Approach Towards CGG Repeat Expansion in FMR1 Gene in Systemic Lupus Erythematosus and in Sjögren’s Syndrome: A Preliminary Report

  • B. Granel
  • V. Ravix
  • K. Pedeillier
  • J. Serratrice
  • P. Disdier
  • M.-A. Voelckel
  • J.-F. Mattei
  • P.-J. Weiller
Original Article
  • 41 Downloads

Abstract:

Co-occurrent autoimmune disease and fragile X syndrome has been reported in the literature and we have therefore studied the expansion of Cytosine-Guanine-Guanine (CGG) repeat in FMR1 gene in a series of females with autoimmune diseases such as systemic lupus erythematosus and Sjo¨gren’s syndrome, with PCR and Southern blot methods. The average length of trinucleotide repeat was not increased in these female patients as compared with controls. These preliminary data on a short series of patients suggest a possible absence of trinucleotide repeat expansion abnormality associated with autoimmune diseases such as systemic lupus erythematosus and Sjo¨gren’s syndrome

Key words:(CGG)n repeat – Fragile X syndrome – Sjo¨gren’s syndrome – Systemic lupus erythematosus 

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Copyright information

© Clinical Rheumatology 2000

Authors and Affiliations

  • B. Granel
    • 1
  • V. Ravix
    • 2
  • K. Pedeillier
    • 2
  • J. Serratrice
    • 1
  • P. Disdier
    • 1
  • M.-A. Voelckel
    • 2
  • J.-F. Mattei
    • 2
  • P.-J. Weiller
    • 1
  1. 1.Service de Médecine Interne, Hôpital d’Adultes de la TimoneFR
  2. 2.Laboratoire de Génétique Moléculaire, Hôpital d’Enfants de la Timone, Marseille, FranceFR

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