agammaglobulinemia 2, autosomal recessive

Agammaglobulinemia 2, autosomal recessive is a rare condition that falls under the group of autosomal agammaglobulinemias. The disease is caused by a mutation in the IGLL1 gene, which is important for the normal development and function of the immune system. This condition has been noted in genetic databases such as OMIM (OMIM:613500) and is indexed in the Genetic and Rare Diseases Information Center (GARD:15672). Although detailed information about the complete range of symptoms and clinical course is not provided here, the definition emphasizes the genetic basis of the condition.

Information about symptoms is currently limited for this condition.

The cause of agammaglobulinemia 2, autosomal recessive is a genetic mutation in the IGLL1 gene. This genetic change interferes with normal immune system development. As the condition is inherited in an autosomal recessive manner, an individual must inherit two copies of the mutated gene to be affected.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about research is currently limited for this condition.