The BLNK deficiency is caused by BLNK gene, a scaffold protein that binds BTK, PLCγ2, Grb2, Vav and Nck and is associated with intracellular calcium mobilization, essential for cell activation. All patients with defects in BLNK have a block in B cell differentiation at the pro-B to pre-B cell transition. Two patients with agammaglobulinemia and defects in BLNK have been identified.
Alternative names
Hypoglobulinemia and absent B cells
Classification
- Deficiencies predominantly affecting antibody production
- Agammaglobulinemia
Inheritance
Autosomal recessive
Cross references
Phenotypically related immunodeficiencies
IDR factfile for X-linked agammaglobulinemia
IDR factfile for X-linked hypogammaglobulinemia with growth hormone deficiency
IDR factfile for Igα deficiency
Incidence
Incidence is not known.