A Rare Form of Chronic Granulomatous Disease (Type Iva) Presenting as Inflammatory Bowel Disease
Neutrophil dysfunction syndromes can sometimes mimic the clinical and pathological features of inflammatory bowel disease. The case of a 3.5-year-old boy with chronic diarrhea, abdominal pain, poor growth since infancy and microcytic, hypochromic anemia is presented. After an extensive diagnostic ev...
Saved in:
Main Author: | Francisco A Sylvester |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
1996-01-01
|
Series: | Canadian Journal of Gastroenterology |
Online Access: | http://dx.doi.org/10.1155/1996/717396 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Granuloma Multiforme: A Rare Granulomatous Disease
by: Yogesh Poudyal, et al.
Published: (2019-01-01) -
Chronic Granulomatous Disease Presenting as Aseptic Ascites in a 2-Year-Old Child
by: J. F. Moreau, et al.
Published: (2013-01-01) -
Current Concepts of Hyperinflammation in Chronic Granulomatous Disease
by: Nikolaus Rieber, et al.
Published: (2012-01-01) -
Inflammatory Bowel Diseases and Irritable Bowel Syndrome: Overlap of Two Nosological Forms or Two Variants of the Same Disease?
by: A. A. Sheptulin, et al.
Published: (2019-12-01) -
Sources of Bias in Common Diagnosis of Chronic Inflammatory Bowel Diseases
by: O. A. Svatkova, et al.
Published: (2020-12-01)