Article
Chromosome 22q11.2 deletion syndrome and DiGeorge syndrome
18 Dec 2018
Abstract excerpt
Chromosome 22q11.2 deletion syndrome is the most common microdeletion syndrome in humans. The effects are protean and highly variable, making a unified approach difficult. Nevertheless, commonalities have been identified and white papers with recommended evaluations and anticipatory guidance have been published. This review will cover the immune system in detail and discuss both the primary features and the...
