Hereditary Deficiency of the Second Component of Complement: Early Diagnosis and 21-Year Follow-Up of a Family

Complement deficiencies are rare and often underdiagnosed primary immunodeficiencies that may be associated with invasive bacterial diseases. Serious infections with encapsulated organisms (mainly Streptococcus pneumoniae, but also Neisseria meningitides and Haemophilus influenzae type B) are freque...

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Bibliographische Detailangaben
Veröffentlicht in:Medicina (Kaunas)
Hauptverfasser: Dellepiane, Rosa Maria, Baselli, Lucia Augusta, Cazzaniga, Marco, Lougaris, Vassilios, Macor, Paolo, Giordano, Mara, Gualtierotti, Roberta, Cugno, Massimo
Format: Artigo
Sprache:Inglês
Veröffentlicht: MDPI 2020
Schlagworte:
Case Report
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7143546/
https://ncbi.nlm.nih.gov/pubmed/32164349
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/medicina56030120
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