Hyper immunoglobulin (Ig) E syndrome is a rare complex immunoregulatory disorder characterized by hyperglobulinemia, recurrent bacterial infections and chronic eczematous dermatitis. The onset of this syndrome may occur at any time from early childhood onwards, and may include eosinophilia and osteoarticular and dental abnormalities. The mortality in untreated patients three years after diagnosis can be high as 75%. Cardiac involvement is the most common cause of increased morbidity and mortality. Early diagnosis of this condition and starting appropriate therapy is of paramount importance in establishing a diagnosis and decreasing the morbidity and mortality associated with this condition.
- Home
- About us
- EDITORIAL BOARD
- INSTRUCTION TO AUTHOR
- Current Issue
- Archive
- September, 2024
- August, 2024
- July 2024
- June 2024
- May 2024
- April 2024
- March 2024
- February 2024
- January 2024
- December 2023
- November, 2023
- October 2023
- September 2023
- August 2023
- July 2023
- June 2023
- May 2023
- April 2023
- March 2023
- February 2023
- January 2023
- December 2022
- November 2022
- October 2022
- September 2022
- August 2022
- July 2022
- June 2022
- May 2022
- April 2022
- March 2022
- February 2022
- January 2022
- December 2021
- November, 2021
- October, 2021
- September, 2021
- August, 2021
- July, 2021
- June, 2021
- May, 2021
- April 2021
- March 2021
- February 2021
- January 2021
- Submit Article
- Certificate
- Reviewers Form
- Contact Us