Clinical and Experimental Pediatrics

Search

Search

Close


Warning: fopen(/home/virtual/pediatrics/journal/upload/ip_log/ip_log_2024-11.txt) [function.fopen]: failed to open stream: Permission denied in /home/virtual/pediatrics/journal/ip_info/view_data.php on line 93

Warning: fwrite(): supplied argument is not a valid stream resource in /home/virtual/pediatrics/journal/ip_info/view_data.php on line 94

All issues > Volume 52(6); 2009

Case Report
Korean J Pediatr. 2009;52(6):721-724. Published online June 15, 2009.
A Korean familial case of hereditary complement 7 deficiency
Moon Kyu MK Ki1, Kyung Yul KY Lee3, Jun Hwa JH Lee2
1Department of Immunology, School of Medicine, Kyungpook National University Hospital, Daegu, South Korea
2Department of Pediatrics, Masan Samsung Hospital, Sungkyunkwan University School of Medicine, Masan, South Korea
3Department of Physical Education, Kyungnam University, Masan, South Korea
Correspondence Jun Hwa JH Lee ,Email: ljh3643@hanmail.net, ljh3643@skku.edu
Abstract
Meningococcal infections can be associated with abnormalities of the complement system, which contains 5 terminal complement proteins. Furthermore, deficiencies in 1 of these 5, complement component 7 (C7), leads to the loss of complement lytic function, and affected patients show increased susceptibility to recurrent meningococcal meningitis and systemic Neisseria gonorrhoeae infection. In September 2003, an 11-year-old female patient presented at our outpatient department with high fever, lower leg pain, headache, and petechiaes. She rapidly progressed to coma but later achieved full recovery due to prompt treatment. Her final diagnosis was meningococcal sepsis and arthritis. Her elder brother also had a similar bacterial meningoencephalitis history, which encouraged us to perform analyses for complement component and gene mutations. Resultantly, both the brother and sister were found to have the same mutation in the C7 gene. Subsequently, vaccinations of the meningococcal vaccine meningococcal vaccine (MenomuneⓇ) were administered. However, in September 2006, the brother expired due to acute micrococcus meningoencephalitis. At present, the 16-year-old female patient is healthy. Here, we report a Korean family with a hereditary C7 deficiency with susceptibility to meningococcal infections due to C7 gene mutation.

Keywords :Meningococcal infection, Complement 7 deficiency, Korean, C7 gene mutation, Meningococcal vaccine

Go to Top