First reported case of Omenn syndrome in a patient with reticular dysgenesis

Ítems similars

• Reticular dysgenesis: international survey on clinical presentation, transplantation, and outcome
  per: Hoenig, Manfred, et al.
  Publicat: (2017)
• Reticular dysgenesis–associated AK2 protects hematopoietic stem and progenitor cell development from oxidative stress
  per: Rissone, Alberto, et al.
  Publicat: (2015)
• Novel Presentation of Omenn Syndrome in Association with Aniridia
  per: Sheehan, William J., et al.
  Publicat: (2009)
• RAG1 reversion mosaicism in a patient with Omenn syndrome
  per: Crestani, Elena, et al.
  Publicat: (2014)
• Expanding the spectrum of recombination-activating gene 1 deficiency: A family with early-onset autoimmunity
  per: Henderson, Lauren A., et al.
  Publicat: (2013)