Velocardiofacial syndrome
MONDO:0008644A chromosomal disease that has material basis in deletion polymorphisms at chromosome location 22q11 and is characterized by variable developmental problems and schizoid features.
Also known as: 22q11 deletion syndrome, Shprintzen VCF syndrome, VCF syndrome, deletion 22q11.2 syndrome, velocardiofacial syndrome, Shprintzen syndrome, chromosome 22Q11.2 deletion syndrome
4 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
-
New study tests medications for brain symptoms in three genetic disorders
Disease control Recruiting nowThis study looks at thinking and mental health issues in people with Velocardiofacial, Williams, and Fragile X syndromes. Researchers will test how well medications like methylphenidate, fluoxetine, and risperidone improve these symptoms. The goal is to better understand and trea…
Phase: PHASE4 • Sponsor: The Chaim Sheba Medical Center • Aim: Disease control
Last updated Jun 27, 2026 11:03 UTC
-
A common antidepressant may tame anxiety in kids with autism and ADHD — a trial puts it to the test
Symptom relief Recruiting nowThis trial tests whether sertraline, a widely used antidepressant, can reduce anxiety in children and teens aged 8 to 17 with neurodevelopmental disorders such as autism, ADHD, Fragile X syndrome, and Tourette syndrome. Participants receive either sertraline or a placebo for seve…
Phase: PHASE2 • Sponsor: Holland Bloorview Kids Rehabilitation Hospital • Aim: Symptom relief
Last updated Jul 29, 2026 00:00 UTC
-
Could a headset boost brainpower in teens with a rare genetic condition?
Symptom relief Recruiting nowThis study tests whether a gentle brain stimulation technique called tACS, used at home for 5 days a week over 4 weeks, can improve memory and thinking in 40 young people aged 14-25 with 22q11.2 deletion syndrome. The stimulation is personalized based on each participant's MRI an…
Phase: NA • Sponsor: Stephan Eliez • Aim: Symptom relief
Last updated Jun 27, 2026 08:01 UTC