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  Vol. 144 No. 7, July 1984 TABLE OF CONTENTS
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Recurrent Neisseria meningitidis Bacteremia

Association With Deficiency of the Eighth Component of Complement (C8) in a Sephardic Jewish Family

Ari Zimran, MD; Oded Kuperman, PhD; Ovadia Shemesh, MD; Chaim Hershko, MD

Arch Intern Med. 1984;144(7):1481-1482.


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.

(Arch Intern Med 1984;144:1481-1482)



Author Affiliations



From the Department of Medicine (Drs Zimran, Shemesh, and Hershko) and the Immunology Laboratory (Dr Kuperman), Shaare Zedek Medical Center and Hebrew University Medical School, Jerusalem.


Footnotes



Accepted for publication Aug 29, 1983.

Reprint requests to Shaare Zedek Medical Center, Jerusalem, Israel (Dr Hershko).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

C5 Deficiency in a White Family
Boelaert et al.
Arch Intern Med 1985;145:1333-1334.
ABSTRACT  





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