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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Detalhes bibliográficos
Publicado no:Medicina (Kaunas)
Main Authors: Dellepiane, Rosa Maria, Baselli, Lucia Augusta, Cazzaniga, Marco, Lougaris, Vassilios, Macor, Paolo, Giordano, Mara, Gualtierotti, Roberta, Cugno, Massimo
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2020
Assuntos:
Case Report
Acesso em linha: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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