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AĞIR KOMBİNE İMMÜN YETMEZLİK: OLGU SUNUMU

Year 2003, Volume: 4 Issue: 3, 25 - 27, 17.09.2003

Abstract

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References

  • 1. Lin JS, Shyur SD, Lin HY. Severe combined immunodeficiency with B-lymphocytes (T-B+SCID): report of two cases. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi 1998; 39: 406-11.
  • 2. Buckley RH. Advances in the understanding and treatment of human severe combined immunodeficiency. Immunol Res 2001; 22: 237-51.
  • 3. Buckley RA.The Immunologic System and disorders. In: Behrman RE, Kliegman RM, Jenson HB (eds). Nelson Textbook of Pediatrics, 16 ed. Pennsylvania W.B.Saunders Company, 2000: 602-3.
  • 4. Fanos JH, Puck JM. Family pictures: growing up with a brother with X linked severe combined immunodeficiency.Am J Med Genet 2001; 98: 57-63.
  • 5. Gaspar HG, Gilmour KC, Jones AM. Severe combined immunodeficiency-molecular pathogenesis and diagnosis.Arch Dis Child 2001; 84:169-73.
  • 6. Stocs RM, Thompson JW, Church JA, Kun S, Simms E. Severe combined immunodeficiency: Otolaryngological presentation and management. Ann Otol Rhinol Larýngol1999;108: 403-407.
  • 7. Gennery AR, Cant AJ. Diagnosis of severe combined immunodeficiency. J Clin Pathol 2001; 54:191-5.
  • 8. Hague RA, Rassam S, Morgan G, Cant AJ. Early diagnosis of severe combined immunodeficiency syndrome.Arch Dis Child 1994; 70: 260-3.
  • 9. European Society for Immunodeficiencies. Severe Combined Immunodeficiency. ESID Newsletter 10, 2000:8.
  • 10. Fontan Casariego G. Primary immunodeficiencies. Clinical features and variant forms. Allergol Immunopathol (madr) 2001; 29:101-7.

A Case Of Severe Combined Immunodeficiency

Year 2003, Volume: 4 Issue: 3, 25 - 27, 17.09.2003

Abstract

Severe combined immunodeficiency (SCID) is a heterogeneous group of inherited disorders characterized byprofound abnormalities in T, B and natural killer cell development and function, resulting in failure of bothcellular and humoral immunity. The age of presentation is variable but occurs typically between 3 and 6 months.The major clinical manifestations include recurrent diarrhea, persistant oral candidiasis, pneumonia, recurrentotitis media, cutaneous fungal infections and sepsis. Opportunistic infection induced end organparticularly to the lungs and liver, is associated with greatly increased morbidity and mortality. Therefore SCIDhas been described as a pediatric emergency.In this article a 5-month-old female infant admitted with the complaint of recurrent respiratory infectionsand disseminated fungal infections and diagnosed as severe combined immunodeficiency (SCID) ispresented

References

  • 1. Lin JS, Shyur SD, Lin HY. Severe combined immunodeficiency with B-lymphocytes (T-B+SCID): report of two cases. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi 1998; 39: 406-11.
  • 2. Buckley RH. Advances in the understanding and treatment of human severe combined immunodeficiency. Immunol Res 2001; 22: 237-51.
  • 3. Buckley RA.The Immunologic System and disorders. In: Behrman RE, Kliegman RM, Jenson HB (eds). Nelson Textbook of Pediatrics, 16 ed. Pennsylvania W.B.Saunders Company, 2000: 602-3.
  • 4. Fanos JH, Puck JM. Family pictures: growing up with a brother with X linked severe combined immunodeficiency.Am J Med Genet 2001; 98: 57-63.
  • 5. Gaspar HG, Gilmour KC, Jones AM. Severe combined immunodeficiency-molecular pathogenesis and diagnosis.Arch Dis Child 2001; 84:169-73.
  • 6. Stocs RM, Thompson JW, Church JA, Kun S, Simms E. Severe combined immunodeficiency: Otolaryngological presentation and management. Ann Otol Rhinol Larýngol1999;108: 403-407.
  • 7. Gennery AR, Cant AJ. Diagnosis of severe combined immunodeficiency. J Clin Pathol 2001; 54:191-5.
  • 8. Hague RA, Rassam S, Morgan G, Cant AJ. Early diagnosis of severe combined immunodeficiency syndrome.Arch Dis Child 1994; 70: 260-3.
  • 9. European Society for Immunodeficiencies. Severe Combined Immunodeficiency. ESID Newsletter 10, 2000:8.
  • 10. Fontan Casariego G. Primary immunodeficiencies. Clinical features and variant forms. Allergol Immunopathol (madr) 2001; 29:101-7.
There are 10 citations in total.

Details

Other ID JA96SV62RT
Journal Section Case Report
Authors

Nesrin Gülez This is me

Hasan Ağın This is me

Şebnem Çalkavur This is me

Yeşim Ergüdenler This is me

Ferah Genel This is me

Mustafa Bak This is me

Publication Date September 17, 2003
Published in Issue Year 2003 Volume: 4 Issue: 3

Cite

EndNote Gülez N, Ağın H, Çalkavur Ş, Ergüdenler Y, Genel F, Bak M (September 1, 2003) A Case Of Severe Combined Immunodeficiency. Meandros Medical And Dental Journal 4 3 25–27.