IgA nephropathy in a child with X-linked agammaglobulinemia: a case report
Abstract Background X-linked agammaglobulinemia (XLA) is a primary immunodeficiency disease caused by mutations in the Bruton tyrosine kinase (BTK) gene. Individuals diagnosed with XLA are at an increased risk of developing autoimmune diseases. However, renal involvement are rare in cases of XLA. Ca...
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| Main Authors: | , , , , |
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| Format: | Book |
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BMC,
2024-04-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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