The 22q11 microdeletion is associated with DiGeorge or velocardiofacial (VCFS) syndrome which is an autosomal dominant condition with variable expressivity ...

We provide individualized diagnostic and management services in genetics, cardiology, plastic and reconstructive surgery, speech-language pathology, ...

Founded in 1996, the 22q and You Center is the premiere site for the diagnosis and multidisciplinary management of children with a chromosome 22q11.2 deletion.

Individuals with 22q11.2 deletion syndrome (22q11.2DS) can present with a wide range of features that are highly variable, even within families.

Dec 1, 2019 · The deletion occurs near the middle of the chromosome at a location designated q11.2. 22q11.2 deletion syndrome has many possible signs and ...

22q deletion syndrome can affect any system of the body, however most children with 22q have heart, immune, learning, speech, and/or behavior difficulties.

22q11.2 deletion syndrome (22qDS) is a genetic syndrome associated with a chromosome 22q11.2 deletion and variable phenotypic expression that commonly ...

Seattle Children's 22q Clinic brings together experts in many fields to care for children who have differences in a part of chromosome 22 called q11.2.