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