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العنوان
Study of Interleukin 23 Gene polymorphism in egyptian patients with allergic Rhinitis /
المؤلف
Mahmoud, Mona Hussein.
هيئة الاعداد
باحث / منى حسين محمود
مشرف / قاسم محمد قاسم
مناقش / محسن محمود عبد الرازق
مناقش / حماده فضل هاشم
الموضوع
Ophthalmology congresses. Otolaryngology congresses.
تاريخ النشر
2019.
عدد الصفحات
86 p. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
الحنجرة
تاريخ الإجازة
1/1/2019
مكان الإجازة
جامعة بنها - كلية طب بشري - الانف والاذن والحنجره
الفهرس
Only 14 pages are availabe for public view

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from 86

Abstract

The development of allergic rhinitis (AR) is caused by the interaction between genetic predisposition and environmental factors. Recent investigations have begun to identify genes that might be involved in AR The genes encoding cytokines and receptors in patients with AR were investigated the most . several studies have investigated single-nucleotide polymorphisms (SNPs) in genes encoding the molecules implicated in the pathogenesis of allergic rhinitis; including specific interleukins (ILs) and their receptors. Until recently it has been assumed that development and manifestation of allergic airway disease was primarily influenced by the activity of T helper (Th)1, Th2 cells and T-regulatory (Treg) cells in genetically susceptible individuals As observed in recent studies, several SNPs in the IL-23R gene are found to be associated with immune-related diseases, including Crohn’s disease, rheumatoid arthritis, Behcet’s disease, and ankylosing spondylitis This study aimed at is to investigate the association between IL-23gene polymorphisms and susceptibility to allergic rhinitis. This study included 100 patients of allergic rhinitis as case group and 75 healthy s ubject as control group collected between January 2017 and March 2017 Peripheral venous blood samples obtained under complete aseptic conditions and maximum precautions and applied into vacutainer tubes containing EDTA and stored at – 80 for molecular assay of IL 23 R genotypes.