r/22q: A message board for discussion and sharing of information related to 22q.11.2 deletion syndrome (aka DiGeorge syndrome) and other forms of 22Q…

Dec 13, 2023 · 22q11.2 is DiGeorge syndrome. It has noticeable features, one of which being cardiac defects. A common cardiac defect with that syndrome is ...

Apr 13, 2022 · I just want our baby boy to be healthy. This has sucked all the joy out of finally getting pregnant after trying for 7 years. All 3 ultrasounds ...

May 3, 2024 · Tested high risk for 22q11.2 deletion (DiGeorge Syndrome). 12+3 - Ultrasound and meeting with genetic counsellor. Ultrasound showed no ...

The major clinical manifestations of 22q11.2DS include congenital heart disease, particularly conotruncal malformations (ventricular septal defect, tetralogy of ...

Apr 5, 2023 · I received my NIPT results at 12 weeks with a high risk for DiGeorge Syndrome. That call was one of the worst moments of my life.

2 deletion syndrome is a genetic defect caused by a microdeletion on the long arm (q arm) of the 22 chromosome. Outcomes for Patients with 22q Deletion Syndrome.

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, ...