Publication:
Bruton’s X-Linked Agammaglobulinemia Presenting as Chronic Monoarticular Arthritis

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorKumar, Mani Kant
dc.contributor.authorPatel, Pankaj Kumar
dc.contributor.authorTahir, Mohammad Mahtab Ali
dc.date.accessioned2026-05-25T07:58:58Z
dc.date.available2026-05-25T07:58:58Z
dc.date.issued2012
dc.descriptionMani Kant Kumar Assistant Professor, Narayan Medical College and Hospital, Jamuhar, Sasaram, Bihar Pankaj Kumar Patel Assistant Professor, Department of Pathology, Narayan Medical College and Hospital, Jamuhar, Sasaram, Bihar Mohammad Mahtab Ali Tahir Junior Resident, Department of Paediatrics, Narayan Medical College and Hospital, Jamuhar, Sasaram, Bihar
dc.description.abstractAbstract: Bruton’s X-Linked Agammaglobulinemia (XLA) is an X linked recessive primary immune deficiency disorder characterized by recurrent bacterial infections and failure to generate immunoglobulins of all isotypes due to the absence or profoundly decreased mature B cells and plasma cells, secondary to mutations in the Bruton’s tyrosine kinase (Btk) gene. The coexistence of chronic monoarticular arthritis in a patient with Bruton’s XLA has been described an uncommon presentation. We describe a 5 year-old boy with XLA and chronic monoarticular arthritis.
dc.identifierhttps://doi.org/10.3126/jnps.v32i3.6183
dc.identifier.urihttps://hdl.handle.net/20.500.14572/6240
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectBruton’s X-linked Agammaglobulinemia
dc.subjectChronic monoarticular arthritis
dc.subjectBtk gene
dc.titleBruton’s X-Linked Agammaglobulinemia Presenting as Chronic Monoarticular Arthritis
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage249
oaire.citation.startPage245
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relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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