ArticlePediatric cardiology2008
Chronic granulomatous disease associated with atypical Kawasaki disease.
Article in Pediatric cardiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
12 citing papers in PubMed, 19 citations in OpenAlex.
- Kawasaki Disease and Inborn Errors of Immunity: Exploring the Link and Implications.Diagnostics (Basel, Switzerland) · 2023Review
- X-Linked Agammaglobulinemia with Kawasaki Disease.Indian journal of pediatrics · 2022Article
- Genetic, Immunological, and Clinical Features of the First Mexican Cohort of Patients with Chronic Granulomatous Disease.Journal of clinical immunology · 2020Article
- Kawasaki disease and immunodeficiencies in children: case reports and literature review.Rheumatology international · 2019Review
- p47Journal of clinical immunology · 2018Review
- A child with X-linked agammaglobulinemia and Kawasaki disease: an unusual association.Rheumatology international · 2017Review
- Presence of a Juvenile Idiopathic Arthritis and Chronic Granulomatous Disease in a Child.Iranian journal of pediatrics · 2015Article
- Reactive oxygen species deficiency induces autoimmunity with type 1 interferon signature.Antioxidants & redox signaling · 2014Article
- Kawasaki disease in a girl with Turner syndrome: a remarkable association.Italian journal of pediatrics · 2014Article
- Kawasaki's disease: An unusual presentation.Journal of cardiovascular disease research · 2012Article
- NADPH oxidase controls phagosomal pH and antigen cross-presentation in human dendritic cells.Blood · 2008Article
- Inflammatory manifestations in chronic granulomatous disease (CGD).Journal of clinical immunology · 2008Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Chronic granulomatous disease (CGD) is an infrequent inherited disorder characterized by recurrent infections and abnormal granuloma formation. Patients with CGD have an exuberant inflammatory response and an increased risk of developing autoimmunity. We present the case of a 1-year-old boy with CGD who developed several of the characteristic clinical features of Kawasaki Disease. His illness responded to intravenous immunoglobulin, aspirin, and corticosteroids.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.