The Dalglish Family Hearts & Minds Clinic for 22q11.2 Deletion Syndrome

Just in time for 22q Awareness month, The American Journal of Medical Genetics published a special issue on 22q11.2 on October 31^st, 2018. Here is the wonderful collection of articles.

The Dalglish Family 22q Clinic team members were involved in the following studies:

• Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series

• Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects

Our international colleagues published the following studies:

• 22q11.2 deletion syndrome: A tiny piece leading to a big picture

• What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia

• Molecular genetics of 22q11.2 deletion syndrome

• Variable immune deficiency related to deletion size in chromosome 22q11.2 deletion syndrome

• Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well‐established knowledge to new frontiers

• Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review

• The 22q11.2 deletion syndrome: Cancer predisposition, platelet abnormalities and cytopenias

• Otolaryngological features in a cohort of patients affected with 22q11.2 deletion syndrome: A monocentric survey

• Club foot in association with the 22q11.2 deletion syndrome: An observational study

• Neurodevelopmental outcome in 22q11.2 deletion syndrome and management

• The impact of hypocalcemia on full scale IQ in patients with 22q11.2 deletion syndrome

• Longitudinal perspectives on the psychosis spectrum in 22q11.2 deletion syndrome

• 22q and two: 22q11.2 deletion syndrome and coexisting conditions

• The psychosocial impact of 22q11 deletion syndrome on patients and families: A systematic review