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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Medicina (Kaunas)
Päätekijät: Dellepiane, Rosa Maria, Baselli, Lucia Augusta, Cazzaniga, Marco, Lougaris, Vassilios, Macor, Paolo, Giordano, Mara, Gualtierotti, Roberta, Cugno, Massimo
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: MDPI 2020
Aiheet:
Case Report
Linkit: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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