Conditions / Genetic

leukocyte adhesion deficiency 1

info ยท Genetic

A leukocyte adhesion deficiency that has_material_basis_in mutation of the ITGB2 gene on chromosome 21q22.3.

Signs and symptoms

  • Gingivitis
  • Hyperfibrinogenemia
  • Delayed umbilical cord separation
  • Elevated circulating C-reactive protein concentration
  • Recurrent infections
  • Recurrent mucocutaneous candidiasis
  • Recurrent bacterial infections
  • Chronic diarrhea
  • Increased total leukocyte count
  • Poor wound healing

Also known as: LAD1; LFA1 immunodeficiency; leukocyte adhesion deficiency type I; lymphocyte function-associated antigen 1 immunodeficiency