Copy For Citation
Kasap Cuceoglu M., Sener S., Batu E. D., Kaya Akca U., Demir S., Sag E., ...More
SEMINARS IN ARTHRITIS AND RHEUMATISM, vol.51, no.3, pp.559-564, 2021 (SCI-Expanded)
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Publication Type:
Article / Review
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Volume:
51
Issue:
3
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Publication Date:
2021
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Doi Number:
10.1016/j.semarthrit.2021.04.009
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Journal Name:
SEMINARS IN ARTHRITIS AND RHEUMATISM
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Journal Indexes:
Science Citation Index Expanded (SCI-EXPANDED), Scopus, CINAHL, EMBASE, MEDLINE
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Page Numbers:
pp.559-564
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Keywords:
Polyarteritis nodosa, Deficiency of adenosine deaminase 2, Systematic review, Child, immunosuppressants, Biological therapies, Outcome measures, Vasculitis, ADENOSINE-DEAMINASE 2, PHENOTYPIC VARIABILITY, PEDIATRIC VASCULITIS, ADA2 DEFICIENCY, CASE SERIES, CHILDREN, DISEASE, MUTATIONS, GENOTYPE, CLASSIFICATION
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Hacettepe University Affiliated:
Yes
Abstract
Background: Diagnosis of childhood polyarteritis nodosa (PAN) has become challenging after the definition of deficiency of adenosine deaminase 2 (DADA2). We aimed to define the differential features of pediatric PAN and DADA2 patients in our center and in the literature.