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Open access Aug 2026

Persistent Hypogammaglobulinemia Following Anti-CD20 Therapy in a Patient with 22q11.2 Deletion Syndrome: A Case Report

22q11.2 deletion syndrome (22q11.2 DS) is one of the most common microdeletion syndromes, characterized by congenital anomalies and variable immune dysfunction secondary to thymic hypoplasia. The resulting immune dysregulation frequently predisposes affected individuals to autoimmune manifestations, including immun...

Ana Drazic, S. Pasic, Maja Stojanović et al. · 0 citations
Open access Aug 2026

Recurrent Severe Infections and Bronchiectasis in a Heterozygous CFTR Mutation Carrier: A Case Report

Cystic fibrosis (CF) is associated with impaired innate immune function, including dysfunction of circulating monocytes and macrophages, and is currently classified within group V inborn errors of immunity. Emerging evidence suggests that heterozygous CFTR variants may also contribute to immune dysregulation and in...

Stefan Kotlajić, T. Grba, Gordana Petrović et al. · 0 citations

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