Case Report: Symptomatic Chronic Granulomatous Disease in the Newborn.
chronic granulomatous disease
early onset
neonate
outcome
symptoms
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2021
2021
Historique:
received:
03
02
2021
accepted:
08
03
2021
entrez:
15
4
2021
pubmed:
16
4
2021
medline:
21
10
2021
Statut:
epublish
Résumé
Chronic granulomatous disease (CGD) is a primary immunodeficiency, which is diagnosed in most patients between one and three years of age. Here we report on a boy who presented at birth with extensive skin lesions and lymphadenopathy which were caused by CGD. An analysis of the literature revealed 24 patients with CGD who became symptomatic during the first six weeks of life. Although pulmonary complications and skin lesions due to infection were the leading symptoms, clinical features were extremely heterogenous. As follow-up was not well specified in most patients, the long-term prognosis of children with very early onset of CGD remains unknown.
Identifiants
pubmed: 33854515
doi: 10.3389/fimmu.2021.663883
pmc: PMC8039294
doi:
Substances chimiques
Biomarkers
0
Types de publication
Case Reports
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
663883Informations de copyright
Copyright © 2021 Miladinovic, Wittekindt, Fischer, Gradhand, Kunzmann, Zimmermann, Bakhtiar, Klingebiel, Schlösser and Lehrnbecher.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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