A clinical case of autosomal recessive agammaglobulinemia with B-cell deficiency

Background. Primary agammaglobulinemia is the result of specific changes in B-cells that lead to low antibody production. A preliminary diagnosis is established if there is a history of frequent bacterial infections (otitis media, sinusitis, skin abscesses), including severe course, in some cases ca...

Celý popis

Podrobná bibliografie

Hlavní autoři:	E. V. Negodnova, M. S. Iskandyarova, E. N. Tyagusheva, O. A. Radaeva, G. V. Fominova
Médium:	Artigo
Jazyk:	Russo
Vydáno:	Association of Paediatric Allergists and Immunologists of Russia (APAIR) 2024-01-01
Edice:	Аллергология и Иммунология в Педиатрии
Témata:	primary immunodeficiency agammaglobulinemia autosomal recessive form children clinical case
On-line přístup:	https://adair.elpub.ru/jour/article/view/120
Tagy:	Přidat tag Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!