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Progressive Neurodegeneration in Patients with Primary Immunodeficiency Disease on IVIG Treatment

✍ Scribed by Ulrike H.M. Ziegner; Roger H. Kobayashi; Charlotte Cunningham-Rundles; Teresa Español; Anders Fasth; Anna Huttenlocher; Paul Krogstad; Lars Marthinsen; Luigi D. Notarangelo; Srdjan Pasic; Christian H.L. Rieger; Peter Rudge; Raman Sankar; Ann O. Shigeoka; E.Richard Stiehm; Kathleen E. Sullivan; A.David Webster; Hans D. Ochs

Book ID
118768500
Publisher
Elsevier Science
Year
2002
Tongue
English
Weight
172 KB
Volume
102
Category
Article
ISSN
1090-2341

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## Abstract X‐linked agammaglobulinemia (XLA) is a primary immunodeficiency disorder caused by a mutation in the Bruton agammaglobulinemia tyrosine kinase gene that results in severe B‐cell deficiency. So far, neurological complications of XLA have been primarily related to acute and/or chronic cen