شنبه 3 آذر 1403
دوره 2، شماره 1 - ( 11-1392 )
جلد 2 شماره 1 صفحات 46-39 |
برگشت به فهرست نسخه ها
Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
Ghaffari J, Ahanchian H, Zandieh F. Update on Hyper IgE syndrome (HIES). J. Pediatr. Rev 2014; 2 (1) :39-46
URL: http://jpr.mazums.ac.ir/article-1-65-fa.html
URL: http://jpr.mazums.ac.ir/article-1-65-fa.html
Update on Hyper IgE syndrome (HIES). Journal of Pediatrics Review. 1392; 2 (1) :39-46
چکیده: (17764 مشاهده)
Hyper IgE Syndrome (HIES) is a rare primary immunodeficiency disease. Most of HIES cases are sporadic. HIES type AD is caused by mutation in signal transducer and activator of transcription-3 (STAT-3). A number of mosaicism HIES has been reported that is associated with intermediate phenotype. Autosomal recessive HIES (AR-HIES) is due to mutation in Dock-8 or cytokine sis 8 and TYK2 or tyrosine kinase 2. The common manifestations are atopic eczema, staphylococcal dermatitis, cellulitis and folliculitis (cold dermal abscesses that are not warm, painful and without redness), recurrent pneumonia and pulmonary abscesses, osteopenia and recurrent bone fracture. The diagnosis of standard HIES is based on clinical suspicion. There is no specific treatment for HIES. The treatment should be based on the prevention of developing infections. Prophylactic antibiotics such as cotrimoxazole and IVIG are administered. Hematopoietic stem cell transplantation was done for all types of HIES, but there is a little information and experience about the long term results of this therapy.
نوع مطالعه: Narrative Review |
دریافت: 1392/8/18 | پذیرش: 1392/10/17 | انتشار: 1392/10/17
دریافت: 1392/8/18 | پذیرش: 1392/10/17 | انتشار: 1392/10/17
| بازنشر اطلاعات | |
 |
این مقاله تحت شرایط Creative Commons Attribution-NonCommercial 4.0 International License قابل بازنشر است. |
