Hyper-IgE Syndrome with Bullous Pemphigoid and Esophageal Stricture

Hyper IgE syndrome (HIEs) is a rare primary immune complex deficiency that has diverse clinical manifestations. STAT 3 mutation is the basis of hyper IgE classic syndrome which was associated with abnormalities of the face, teeth, skeleton and connective issue that is not visible on recessive type....

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Bibliographic Details
Main Authors: Laras Budiyani, Adeputri Tanesha Idayu, Ika Prasetya Wijaya, Alvina Widhani
Format: Article
Language:Indonesian
Published: Department of Internal Medicine, Faculty of Medicine Universitas Indonesia-Cipto Mangunkusumo Hospital 2016-06-01
Series:Jurnal Penyakit Dalam Indonesia
Subjects:
Online Access:http://jurnalpenyakitdalam.ui.ac.id/index.php/jpdi/article/view/96/92