DOCK8 deficiency in six Iranian patients

Clin Case Rep. 2016 May 17;4(6):593-600. doi: 10.1002/ccr3.574. eCollection 2016 Jun.

Abstract

DOCK8 deficiency is a rare autosomal recessive combined immunodeficiency with high IgE level, eosinophilia, severe eczema, extensive cutaneous viral, and respiratory bacterial infections, mostly in populations with higher prevalence of consanguinity. Molecular diagnosis of this gene is a useful approach for early diagnosis and timely HSCT due to deleterious consequences.

Keywords: Allergy; DOCK8; autosomal recessive; hyper IgE syndrome.

Publication types

  • Case Reports