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, ...

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

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.

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 ...

Speech and language disorders are hallmark features of 22q11.2 deletion syndrome (22qDS). Learning disabilities, cognitive deficits, palate abnormalities, ...

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

2 distal deletion is a rare genetic condition caused by a tiny missing part of one of the body's 46 chromosomes – chromosome 22. For healthy development, ...