Publication:
Recurrent Pneumococcal Meningitis in Homozygous C3 Deficiency

dc.authorscopusid56450837600
dc.contributor.authorTotan, M.
dc.date.accessioned2020-06-21T09:15:02Z
dc.date.available2020-06-21T09:15:02Z
dc.date.issued2002
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Totan] Mehmet, Department of Pediatrics, Ondokuz Mayis Üniversitesi, Samsun, Turkey, Cumhuriyet mah. Ataturk bul., Turkeyen_US
dc.description.abstractCongenital deficiencies of complement system proteins are rare. A 4-year-old girl was admitted for meningitis. She had had repeated attacks of pneumococcal meningitis and otitis media at the age of 3 years. Analysis of cerebrospinal fluid showed that this meningitis was due to pneumococcal infection. Complement 3 and CH50 values of the proband and her brother were low, while her parents were normal. The patient was given polyvalent pneumococcal and anti-haemophilus vaccines plus ceftriaxone. Recovery was complete after 15 days of antibiotic therapy. This is the first description of a case of recurrent meningitis with C3 and CH50 deficiency in a Turkish family. [Indian J Pediatr 2002; 69 (7) : 625-626].en_US
dc.identifier.doi10.1007/BF02722692
dc.identifier.endpage626en_US
dc.identifier.issn0019-5456
dc.identifier.issn0973-7693
dc.identifier.issue7en_US
dc.identifier.pmid12173704
dc.identifier.scopus2-s2.0-0036635062
dc.identifier.scopusqualityQ1
dc.identifier.startpage625en_US
dc.identifier.urihttps://doi.org/10.1007/BF02722692
dc.identifier.volume69en_US
dc.identifier.wosqualityQ2
dc.institutionauthorTotan, M.
dc.language.isoenen_US
dc.publisherThe Indian Journal of Pediatricsen_US
dc.relation.ispartofIndian Journal of Pediatricsen_US
dc.relation.journalIndian Journal of Pediatricsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChildhooden_US
dc.subjectComplement Deficiencyen_US
dc.subjectPneumococcal Meningitisen_US
dc.titleRecurrent Pneumococcal Meningitis in Homozygous C3 Deficiencyen_US
dc.typeArticleen_US
dspace.entity.typePublication

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