22q11.2 deletion syndrome

Velocardiofacial Syndrome: Symptoms, Causes, and Management A genetic condition called Velocardiofacial Syndrome (VCFS), also called 22q11.2 deletion syndrome, is characterized by a combination of immune system abnormalities, developmental delays, and craniofacial malformations. Know More:

Check your child online and learn about Charge syndrome, including its signs, symptoms, diagnosis, and valuable information.

Estimates of the Prevalence of #Speech and #Motor Speech Disorders in Youth With 22q11.2 Deletion Syndrome. #OpenAccess article in #AJSLP by Adriane L. Baylis & Lawrence D. Shriberg https://on.asha.org/315QkaZ #ASHAJournals #slpeeps #22q112

The American Journal of Medical Genetics - Part A is your primary source for all biological and medical aspects of inherited disorders and birth defects research.

22q awareness

Empowering young women with the rare genetic disorder 22q11.2 Deletion Syndrome to share their lived experience and mental health support needs | Children's Research Network

The Dalglish Family 22q Clinic provides patients with care from healthcare experts from many specialties.

Velo-cardio-facial-syndrome, also known as 22q11.2 deletion syndrome and DiGeorge syndrome, is relatively new; the genetic test to determine if a child has it has only been available since 1994. Educating Children with Velo-Cardio Facial Syndrome (also Known as 22q11.2 Deletion Syndrome and DiGeorge Syndrome), Second Edition, effectively blends the thoughtful research that has transpired within the past 15 years with practical and current educational strategies to better meet the needs of…