A case of bruton disease with progressive ataxia

2026 Preprint Open access

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Authors: arash kalantary, Ali Nikkhah, Elham Pourbakhtyaran, mahshid movaheddi, Zahra Baghery, Sahar Nabilou
DOI: 10.22541/au.176778932.21210882/v1
Cited by: 0

Abstract

Introduction:X-linked agammaglobulinemia (XLA), or Bruton agammaglobulinemia, is an inherited immunodeficiency disease that caused by variations of Bruton tyrosine kinase gene (BTK). In 1952 Bruton, described the disease for the first time, for whom t

Fields of Study & Subjects

Chronic Lymphocytic Leukemia Research Immunodeficiency and Autoimmune Disorders Glycogen Storage Diseases and Myoclonus

Publication details

Publication date
7 January 2026
Document type
Preprint