Literature DB >> 6732408

Recurrent Neisseria meningitidis bacteremia. Association with deficiency of the eighth component of complement (C8) in a Sephardic Jewish family.

A Zimran, O Kuperman, O Shemesh, C Hershko.   

Abstract

A 24-year-old man had repeated episodes of meningococcal meningitis. Selective deficiency of the eighth component of complement (C8) was demonstrated in the patient, his twin brother, and in one of five siblings. As the parents were first cousins of normal phenotype, this pattern is suggestive of an autosomal recessive heredity. The present report brings the total number of patients given the diagnosis of C8 deficiency to 14, and calls attention to the existence of this condition in Jews of Sephardic (Mediterranean) origin.

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Year:  1984        PMID: 6732408     DOI: 10.1001/archinte.144.7.1481

Source DB:  PubMed          Journal:  Arch Intern Med        ISSN: 0003-9926


  4 in total

Review 1.  Recurrent meningitis: a case report.

Authors:  M Ceccarelli; M Balestri; C Fontani; L Lupetti; C Ughi
Journal:  Eur J Pediatr       Date:  1989-06       Impact factor: 3.183

Review 2.  Infectious diseases associated with complement deficiencies.

Authors:  J E Figueroa; P Densen
Journal:  Clin Microbiol Rev       Date:  1991-07       Impact factor: 26.132

3.  Complement component deficiencies and infection: C5, C8 and C3 deficiencies in three families.

Authors:  O Sanal; M Loos; F Ersoy; G Kanra; G Seçmeer; I Tezcan
Journal:  Eur J Pediatr       Date:  1992-09       Impact factor: 3.183

4.  Gene responsible for deficient activity of the beta subunit of C8, the eighth component of complement, is located on mouse chromosome 4.

Authors:  S Tanaka; T Suzuki; M Sakaizumi; Y Harada; Y Matsushima; N Miyashita; Y Fukumori; S Inai; K Moriwaki; H Yonekawa
Journal:  Immunogenetics       Date:  1991       Impact factor: 2.846

  4 in total

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