Large BTK gene mutation in a child with X-linked agammaglobulinemia and polyarthritis.

Dhrubajyoti Sharma,Aman Gupta,Shubham Goel,Madhubala Sharma,Amit Rawat,Surjit Singh

Clinical Immunology（2017）

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摘要

•Polyarthritis as presenting feature in patients with XLA is extremely uncommon.•A novel mutation in BTK gene is described.•Regular replacement IVIG results in resolution of arthritis in patients with XLA.

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