Letter to Editor

  • Dr Sunil Kumar Senior Resident, Department of Pediatrics,Kalpana Chawla Government Meidical College, Karnal (Haryana)
DOI: https://doi.org/10.17511/ijpr.2018.i11.10
Keywords: Children, Hyper IgE syndrome

Abstract

The case report is very abridged. The phenotypic features of child whether fitting into those described for children with Job’s Syndrome, detailed family history of other affected/suspected family members and evaluation for other features of Job’s Syndrome is missing.

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References

1. Hill HR, Ochs HD, Quie PG, Clark RA, Pabst HF, Klebanoff SJ, Wedgwood RJ: Defect in neutrophil granulocyte chemotaxis in Job’s syndrome of recurrent “cold” staphylococcal abscesses. Lancet 1974, 2:617-619.

2. Minegishi Y, Saito M, Tsuchiya S, Tsuge I, Takada H, Hara T, Kawamura N, Ariga T, Pasic S, Stojkovic O, Metin A, Karasuyama H: Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome. Nature 2007, 448:1058-1062.

3. Freeman AF, Kleiner DE, Nadiminti H, Davis J, Quezado M, Anderson V, Puck JM, Holland SM: Causes of death in hyper-IgE syndrome. J Allergy Clin Immunol 2007, 119:1234-1240.

4. Yong PF, Freeman AF, Engelhardt KR, Holland S, Puck JM, Grimbacher B. An update on the hyper-IgEsyndromes. Arthritis research & therapy 2012; 14(6):228.
CITATION
DOI: 10.17511/ijpr.2018.i11.10
Published: 2018-11-30
How to Cite
Dr Sunil Kumar. (2018). Letter to Editor. Pediatric Review: International Journal of Pediatric Research, 5(11), 601-602. https://doi.org/10.17511/ijpr.2018.i11.10
Issue
Vol 5 No 11 (2018): NOVEMBER
Section
Letter to Editor(s)

Copyright (c) 2018 Author (s). Published by Siddharth Health Research and Social Welfare Society

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