Literature DB >> 2707135

[Familial Mediterranean fever in a German family].

H Hawle1, G Winckelmann, C S Kortsik.   

Abstract

A 14-year-old German boy had the characteristic signs and symptoms of familial mediterranean fever with recurrent attacks of fever which ran a uniform course and were self-limiting. Laparoscopy revealed sterile peritonitis and marked humoral inflammatory signs. Each acute phase was confined to three days, alternating with symptom-free intervals which lasted for as long as several months. The boy's father and three other members of the paternal family have had similar disease symptoms. Even in patients who are not members of a predisposed ethnic group familial mediterranean fever should be included in the differential diagnosis as a rare cause of recurrent episodes of fever of unknown aetiology.

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Year:  1989        PMID: 2707135     DOI: 10.1055/s-2008-1066652

Source DB:  PubMed          Journal:  Dtsch Med Wochenschr        ISSN: 0012-0472            Impact factor:   0.628


  5 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.  Gene localization for an autosomal dominant familial periodic fever to 12p13.

Authors:  J Mulley; K Saar; G Hewitt; F Rüschendorf; H Phillips; A Colley; D Sillence; A Reis; M Wilson
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

4.  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

5.  A monoallelic double mutation as a cause for TNF receptor-associated periodic fever syndrome.

Authors:  J Trübenbach; G Wildhardt; J Niebel; H Hawle; Daniela Steinberger
Journal:  Rheumatol Int       Date:  2009-06-23       Impact factor: 2.631

  5 in total

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