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Erschienen in: Journal of Clinical Immunology 7/2022

08.07.2022 | Letter to Editor

Deficiency of Adenosine Deaminase 2 Presenting as Periodic Fever at the Mainland of Familial Mediterranean Fever

verfasst von: Mustafa Çakan, Betül Sözeri

Erschienen in: Journal of Clinical Immunology | Ausgabe 7/2022

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Excerpt

To the Editor …
Literatur
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Zurück zum Zitat Navon Elkan P, Pierce SB, Segel R, Walsh T, Barash J, Padeh S, et al. Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy. N Engl J Med. 2014;370:921–31.CrossRefPubMed Navon Elkan P, Pierce SB, Segel R, Walsh T, Barash J, Padeh S, et al. Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy. N Engl J Med. 2014;370:921–31.CrossRefPubMed
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Zurück zum Zitat Tanatar A, Karadağ ŞG, Sözeri B, Sönmez HE, Çakan M, Kendir Demirkol Y, et al. ADA2 deficiency: case series of five patients with varying phenotypes. J Clin Immunol. 2020;40:253–8.CrossRefPubMed Tanatar A, Karadağ ŞG, Sözeri B, Sönmez HE, Çakan M, Kendir Demirkol Y, et al. ADA2 deficiency: case series of five patients with varying phenotypes. J Clin Immunol. 2020;40:253–8.CrossRefPubMed
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Zurück zum Zitat Pinto B, Deo P, Sharma S, Syal A, Sharma A. Expanding spectrum of DADA2: a review of phenotypes, genetics, pathogenesis and treatment. Clin Rheumatol. 2021;40:3883–96.CrossRefPubMed Pinto B, Deo P, Sharma S, Syal A, Sharma A. Expanding spectrum of DADA2: a review of phenotypes, genetics, pathogenesis and treatment. Clin Rheumatol. 2021;40:3883–96.CrossRefPubMed
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Zurück zum Zitat Meyts I, Aksentijevich I. Deficiency of adenosine deaminase 2 (DADA2): updates on the phenotype, genetics, pathogenesis, and treatment. J Clin Immunol. 2018;38:569–78.CrossRefPubMedPubMedCentral Meyts I, Aksentijevich I. Deficiency of adenosine deaminase 2 (DADA2): updates on the phenotype, genetics, pathogenesis, and treatment. J Clin Immunol. 2018;38:569–78.CrossRefPubMedPubMedCentral
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Zurück zum Zitat Öztürk K, Coşkuner T, Baglan E, Sönmez HE, Yener GO, Çakmak F, et al. Real-life data from the largest pediatric familial mediterranean fever cohort. Front Pediatr. 2022;9:805919.CrossRefPubMedPubMedCentral Öztürk K, Coşkuner T, Baglan E, Sönmez HE, Yener GO, Çakmak F, et al. Real-life data from the largest pediatric familial mediterranean fever cohort. Front Pediatr. 2022;9:805919.CrossRefPubMedPubMedCentral
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Zurück zum Zitat Çakan M, Aktay-Ayaz N, Keskindemirci G, Karadağ ŞG. Two cases of periodic fever syndrome with coexistent mevalonate kinase and Mediterranean fever gene mutations. Turk J Pediatr. 2017;59:467–70.CrossRefPubMed Çakan M, Aktay-Ayaz N, Keskindemirci G, Karadağ ŞG. Two cases of periodic fever syndrome with coexistent mevalonate kinase and Mediterranean fever gene mutations. Turk J Pediatr. 2017;59:467–70.CrossRefPubMed
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Zurück zum Zitat Nihira H, Nakagawa K, Izawa K, Kawai T, Yasumi T, Nishikomori R, et al. Fever of unknown origin with rashes in early infancy is indicative of adenosine deaminase type 2 deficiency. Scand J Rheumatol. 2018;47:170–2.CrossRefPubMed Nihira H, Nakagawa K, Izawa K, Kawai T, Yasumi T, Nishikomori R, et al. Fever of unknown origin with rashes in early infancy is indicative of adenosine deaminase type 2 deficiency. Scand J Rheumatol. 2018;47:170–2.CrossRefPubMed
Metadaten
Titel
Deficiency of Adenosine Deaminase 2 Presenting as Periodic Fever at the Mainland of Familial Mediterranean Fever
verfasst von
Mustafa Çakan
Betül Sözeri
Publikationsdatum
08.07.2022
Verlag
Springer US
Erschienen in
Journal of Clinical Immunology / Ausgabe 7/2022
Print ISSN: 0271-9142
Elektronische ISSN: 1573-2592
DOI
https://doi.org/10.1007/s10875-022-01328-z

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