My boy is 21 weeks old. The Amniocentesis confirm there is no chromosomal abnormalities. But he has been diagnosed by FMC that he has Ventriculomegaly approximately 10mm, thicken cervical skin approximately 8.2 mm, double arch. We are anxiously waiting for his Di George Syndrome results. His mother is also waiting for her IgG and IgM blood tests results. Can anyone of you advice me if there is anything I can do to help my boy such as any procedures that can help him before he is born? Thanks