Invasive meningococcal disease in three siblings with hereditary deficiency of the 8(th) component of complement: evidence for the importance of an early diagnosis

BACKGROUND: Deficiency of the eighth component of complement (C8) is a very rare primary immunodeficiency, associated with invasive, recurrent infections mainly caused by Neisseria species. We report functional and immunochemical C8 deficiency diagnosed in three Albanian siblings who presented with...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Orphanet J Rare Dis
Egile Nagusiak: Dellepiane, Rosa Maria, Dell’Era, Laura, Pavesi, Paola, Macor, Paolo, Giordano, Mara, De Maso, Luca, Pietrogrande, Maria Cristina, Cugno, Massimo
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2016
Gaiak:
Research
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4869260/
https://ncbi.nlm.nih.gov/pubmed/27183977
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-016-0448-5
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