Literature DB >> 17676340

Compound heterozygosity for three common MEFV mutations in a highly consanguineous family with familial Mediterranean fever.

H Seidel1, O K Steinlein.   

Abstract

Consanguinity is not the only factor influencing the occurrence of autosomal recessive disorders such as familial Mediterranean fever (FMF). The extended, multiple consanguineous Turkish pedigree presented here demonstrates that the population frequency of certain mutations (so-called "ancient" mutations) can be at least equally important. In high-risk populations different combinations of mutations can occur within the same family, increasing not only the intrafamilial clinical variability, but also causing considerable recurrence risks even in marriages with unrelated spouses.

Entities:  

Mesh:

Year:  2007        PMID: 17676340     DOI: 10.1007/s00431-007-0572-2

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  4 in total

1.  A candidate gene for familial Mediterranean fever.

Authors: 
Journal:  Nat Genet       Date:  1997-09       Impact factor: 38.330

2.  Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. The International FMF Consortium.

Authors: 
Journal:  Cell       Date:  1997-08-22       Impact factor: 41.582

3.  The fate of 12 recessive mutations in a single village.

Authors:  J Zlotogora; Y Hujerat; S Barges; S A Shalev; A Chakravarti
Journal:  Ann Hum Genet       Date:  2007-03       Impact factor: 1.670

4.  Familial Mediterranean fever: the segregation of four different mutations in 13 individuals from one inbred family: genotype-phenotype correlation and intrafamilial variability.

Authors:  Ruth Gershoni-Baruch; Marwan Shinawi; Hussein Shamaly; Leah Katsinetz; Riva Brik
Journal:  Am J Med Genet       Date:  2002-05-01
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.