Clinical and Genetic Study of X-linked Agammaglobulinemia Patients (The Benefit of Early Diagnosis)

Clinical and Genetic Study of X-linked Agammaglobulinemia Patients (The Benefit of Early Diagnosis)

X-linked agammaglobulinemia (XLA) is a primary immunodeficiency caused by genetic defects in the Bruton tyrosine kinase (Btk) gene. XLA is characterized as an antibody deficiency by recurrent bacterial infections, the absence of peripheral B cells, and profound reductions in all immunoglobulin isot...

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Bibliographic Details
Main Authors: Zahra Alizadeh, Parisa Dashti, Marzieh Mazinani, Maryam Nourizadeh, Leila Shakerian, Shaghayegh Tajik, Masoud Movahedi, Setareh Mamishi, Zahra Pourpak, Mohammad Reza Fazlollahi
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2020-06-01
Series:Iranian Journal of Allergy, Asthma and Immunology
Subjects:
Bruton tyrosine kinase
Early diagnosis
Mutation
X-linked agammaglobulinemia
Online Access:https://ijaai.tums.ac.ir/index.php/ijaai/article/view/2309

Internet

https://ijaai.tums.ac.ir/index.php/ijaai/article/view/2309

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