T-cell immunodeficiency, congenital alopecia, and nail dystrophy

A severe combined immunodeficiency characterized by congenital alopecia, severe T-cell immunodeficiency, and ridging, pitting or curving of all nails that has material basis in homozygous mutation in the FOXN1 gene on chromosome 17q11-q12.

Also known as: FOXN1 deficiency, T-cell immunodeficiency, congenital alopecia, and nail dystrophy, alopecia immunodeficiency, alymphoid cystic thymic dysgenesis, severe T-cell immunodeficiency-congenital alopecia-nail dystrophy syndrome, winged helix deficiency, Pignata Guarino syndrome, T-cell immunodeficiency, congenital alopecia and nail dystrophy

2 clinical trials for this condition and its sub-types, 0 tagged with T-cell immunodeficiency, congenital alopecia, and nail dystrophy itself.