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Disease: T-cell immunodeficiency- congenital alopecia and nail dystrophy

  • A lesson for unraveling complex aspects of novel immunodeficiencies from the human equivalent of the nude/SCID phenotype
  • Congenital Alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency in two sibs
  • Development of the Nude Rabbit Model
  • FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
  • FOXN1 deficient nude severe combined immunodeficiency
  • FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
  • FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
  • Human clinical phenotype associated with FOXN1 mutations
  • Human equivalent of the mouse Nude/SCID phenotype: long-term evaluation of immunologic reconstitution after bone marrow transplantation
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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