Deficiency of complement factor H-related proteins and autoantibody-positive hemolytic uremic syndrome in an infant with combined partial deficiencies and autoantibodies to complement factor H and ADAMTS13

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A 3-month-old male infant developed an extremely severe episode of atypical hemolytic uremic syndrome (aHUS) associated with partial deficiencies of full-length complement factor H (FH; ∼15% of infant normal) and a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAM...

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Detalles Bibliográficos
Autores principales: Michael, Mini, Turner, Nancy, Elenberg, Ewa, Shaffer, Linda G, Teruya, Jun, Arar, Mazen, Hui, Shiu-Ki, Smith, Richard J, Moake, Joel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Rare Diseases
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275444/
https://www.ncbi.nlm.nih.gov/pubmed/30524124
http://dx.doi.org/10.1093/ckj/sfy010

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275444/
https://www.ncbi.nlm.nih.gov/pubmed/30524124
http://dx.doi.org/10.1093/ckj/sfy010

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