Hematopoietic stem cell transplant for hyper-IgM syndrome due to CD40L defects: A single-center experience

Author:

Al-Saud Bandar12,Al-Mousa Hamoud12,Al-Ahmari Ali23,Al-Ghonaium Abdulaziz1,Ayas Mouhab3,Alhissi Safa4,Al-Muhsen Saleh15,Al-Seraihy Amal3,Arnaout Rand12,Al-Dhekri Hasan1,Hawwari Abbas4

Affiliation:

1. Section of Pediatric Allergy/Immunology; Department of Pediatrics; King Faisal Specialist Hospital & Research Center; Riyadh Saudi Arabia

2. Colleges of Medicine; Alfaisal University; Riyadh Saudi Arabia

3. Department of Pediatric Hematology/Oncology; King Faisal Specialist Hospital & Research Center; Riyadh Saudi Arabia

4. Department of Genetics; King Faisal Specialist Hospital & Research Center; Riyadh Saudi Arabia

5. Department of Pediatrics; College of Medicine; King Saud University; Riyadh Saudi Arabia

Publisher

Wiley

Subject

Transplantation,Pediatrics, Perinatology, and Child Health

Reference37 articles.

1. An example of atypical agammaglobulinemia, a case of severe hypogammaglobulinemia with increase of the beta-2 macroglobulin;Burtin;Rev Fr Etud Clin Biol,1961

2. Recurrent bacterial infections and dysgamma-globulinemia: Deficiency of 7S gamma-globulins in the presence of elevated 19S gamma-globulins. Report of two cases;Rosen;Pediatrics,1961

3. Immunodeficiency with hyper-IgM (HIM);Notarangelo;Immunodefic Rev,1992

4. The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome;Aruffo;Cell,1993

5. CD40 ligand gene defects responsible for X-linked hyper-IgM syndrome;Allen;Science,1993

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