Literature DB >> 8366955

[A Dutch family with familial Mediterranean fever].

E J Zweers1, D W Erkelens.   

Abstract

Familial mediterranean fever (or recurrent hereditary polyserositis) is a genetic disorder with an autosomal recessive pattern of inheritance which occurs mostly in patients with eastern Mediterranean origin. Two Dutch patients are described, a 25-year-old women and her 58-year-old father, who suffered from recurring abdominal complaints, fever, and increased erythrocyte sedimentation rate, without evidence of Middle Eastern ancestry or hyperimmunoglobulinemia D.

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Year:  1993        PMID: 8366955

Source DB:  PubMed          Journal:  Ned Tijdschr Geneeskd        ISSN: 0028-2162


  3 in total

1.  Linkage of familial Hibernian fever to chromosome 12p13.

Authors:  M F McDermott; B W Ogunkolade; E M McDermott; L C Jones; Y Wan; K A Quane; J McCarthy; M Phelan; M G Molloy; R J Powell; C I Amos; G A Hitman
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

2.  Autosomal dominant familial Mediterranean fever--like syndrome.

Authors:  C J Mache; U Goriup; N Fischel-Ghodsian; X Chen; J Schwingshandl
Journal:  Eur J Pediatr       Date:  1996-09       Impact factor: 3.183

3.  Exclusion of the familial Mediterranean fever locus as a susceptibility region for autosomal dominant familial Hibernian fever.

Authors:  M F McDermott; E M McDermott; K A Quane; L C Jones; B W Ogunkolade; D Curtis; F Waldron-Lynch; M Phelan; G A Hitman; M G Molloy; R J Powell
Journal:  J Med Genet       Date:  1998-05       Impact factor: 6.318

  3 in total

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