Search In this Thesis
   Search In this Thesis  
العنوان
Association between Interleukin-16 Gene
Polymorphism and Alopecia Areata /
المؤلف
Zahran, Deema Ahmed.
هيئة الاعداد
باحث / ديما أحمذ زهران
مشرف / مصطفى عيادة
مناقش / آمال حسين
مناقش / فادية مصطفى عطية
الموضوع
Dermatology and Venereology.
تاريخ النشر
2015.
عدد الصفحات
93 p. ;
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
الأمراض الجلدية
تاريخ الإجازة
1/1/2015
مكان الإجازة
جامعة قناة السويس - كلية الطب - جلدية وتناسلية
الفهرس
Only 14 pages are availabe for public view

from 110

from 110

Abstract

Alopecia areata (AA) is a recurrent non-scarring type of hair loss that can affect any hair-bearing area and can manifest in many different patterns. Although it is a benign condition and most patients are asymptomatic, it can cause emotional and psychosocial distress. Its prevalence in the general population is 0.1-0.2%. The lifetime risk of developing AA is estimated to be 1.7% and it is responsible for 0.7-3% of patients seen by dermatologists (Karadag-Köse and Güleç 2012).
Alopecia areata (AA) most often is asymptomatic, but some patients (14%) experience a burning sensation or pruritus in the affected area. The condition usually is localized when it first appears. It appears as a single patch in 80% of the patients, two patches in 2.5% and multiple patches in 7.7%. No correlation exists between the number of patches at onset and subsequent severity. AA can affect any hair-bearing area, and more than one area can be affected at once. Frequency of involvement at particular sites is as follows; scalp (66.8-95%), beard of males (28%), eyebrows (3.8%), and extremities (1.3%) (Bolduc and Elston 2015).