مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Verion

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

1,245
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

0
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

GENOTYPE– PHENOTYPE CORRELATION IN PATIENTS WITH FAMILIAL MEDITERRANEAN FEVER: EVALUATION OF E148Q AND M694V MUTATIONS

Pages

  39-47

Abstract

 Background and Objective: FAMILIAL MEDITERRANEAN FEVER (FMF) is an autosomal recessive disorder characterized by self-limited episodes of fevere and painful recurrent polyserositis that predominantly affects Mediterranean races. In recent years some reports have shown high prevalence of FMF in North-west IRAN, with M694V and E148Q being most frequent reported mutations. The aim of this study is to evaluate the clinical MANIFESTATIONs of FMF in patients with these mutations.Materials and Methods: A cross sectional- descriptive study was performed in a 1 year period (January 2007 – January 2008). 71 patients younger than 18 years with clinical diagnosis of disease proved in Children Hospital of Tabriz-Iran were referred to genetic lab for mutation analysis. ARMS-PCR & PCR-RFLP were used to detect mutations. Only 45 patients were shown to have identified mutations and 41 patients among them had M694V and E148Q mutations which were assessed for various clinical MANIFESTATIONs.Results: M694V and E148Q mutations were seen in 55.7% and 35.5% patients respectively. Patients homozygous for M694V were found to have earlier age of onset, longer duration of attacks, higher prevalence of positive family history and more complications. In our patients, prevalence of some MANIFESTATIONs differed from other ethnic groups reported previously.Conclusions: M694V mutation in FMF patients especially in homozygous state is accompanied with more severe disease and more complications.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    RAFIEI, MANDANA, JABARPOUR BONYADI, MORTEZA, GHAFARPOUR SAKHA, K., SAMADI AFSHAR, A., & ESMAIELI, M.. (2008). GENOTYPE– PHENOTYPE CORRELATION IN PATIENTS WITH FAMILIAL MEDITERRANEAN FEVER: EVALUATION OF E148Q AND M694V MUTATIONS. JOURNAL OF ADVANCES IN MEDICAL AND BIOMEDICAL RESEARCH, 16(63), 39-47. SID. https://sid.ir/paper/61105/en

    Vancouver: Copy

    RAFIEI MANDANA, JABARPOUR BONYADI MORTEZA, GHAFARPOUR SAKHA K., SAMADI AFSHAR A., ESMAIELI M.. GENOTYPE– PHENOTYPE CORRELATION IN PATIENTS WITH FAMILIAL MEDITERRANEAN FEVER: EVALUATION OF E148Q AND M694V MUTATIONS. JOURNAL OF ADVANCES IN MEDICAL AND BIOMEDICAL RESEARCH[Internet]. 2008;16(63):39-47. Available from: https://sid.ir/paper/61105/en

    IEEE: Copy

    MANDANA RAFIEI, MORTEZA JABARPOUR BONYADI, K. GHAFARPOUR SAKHA, A. SAMADI AFSHAR, and M. ESMAIELI, “GENOTYPE– PHENOTYPE CORRELATION IN PATIENTS WITH FAMILIAL MEDITERRANEAN FEVER: EVALUATION OF E148Q AND M694V MUTATIONS,” JOURNAL OF ADVANCES IN MEDICAL AND BIOMEDICAL RESEARCH, vol. 16, no. 63, pp. 39–47, 2008, [Online]. Available: https://sid.ir/paper/61105/en

    Related Journal Papers

    Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button