A novel mutation in NCF2 resulting in very-early-onset colitis and juvenile idiopathic arthritis in a patient with chronic granulomatous disease
Abstract Background Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disorder caused by a defect in the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase complex. The disease primarily presents with recurrent infections, and patients may also present with inflammatory...
Main Author: | Suzan AlKhater |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2019-11-01
|
Series: | Allergy, Asthma & Clinical Immunology |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s13223-019-0386-6 |
Similar Items
-
New onset colitis in an adult patient with chronic granulomatous disease treated with hematopoietic stem cell transplantation: a diagnostic dilemma
by: Kara Robertson, et al.
Published: (2018-05-01) -
Idiopathic granulomatous gastritis with severe gastrointestinal bleeding
by: Nazim Gures, et al.
Published: (2016-01-01) -
Idiopathic granulomatous hypophysitis: A report of an uncommon disorder
by: Shubhangi Vinayak Agale, et al.
Published: (2018-01-01) -
Very Early-Onset Inflammatory Manifestations of X-Linked Chronic Granulomatous Disease
by: Roxane Labrosse, et al.
Published: (2017-09-01) -
Systemic juvenile idiopathic arthritis versus adult-onset Still´s disease: the pertinence of changing the current classification criteria
by: Joana Ribeiro Silva, et al.
Published: (2020-04-01)