Jan 13, 2024 · DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a condition caused when a small part of chromosome 22 is missing. This deletion causes several body …

DiGeorge syndrome may be first spotted when an affected newborn has heart defects or convulsions from hypocalcemia due to malfunctioning parathyroid glands and low levels of …

Nov 14, 2025 · DiGeorge syndrome (22q11.2 deletion syndrome) is a genetic condition that occurs when your child is missing a piece of chromosome 22. The condition can affect many …

Boston Children’s Hospital provides a wide range of diagnostic, treatment, consultation, and advocacy services for children with 22q11.2 deletion syndrome. Our experts are experienced …

Jun 5, 2025 · DiGeorge syndrome is a disorder due to a deletion from the 22nd chromosome. Learn about the causes, symptoms, and treatment.

An overview of DiGeorge Syndrome (DGS) symptoms, diagnosis, treatment and management written by experts in allergy, asthma and immunology.

22q11.2 deletion syndrome has many possible signs and symptoms that can affect almost any part of the body. The features of this syndrome vary widely, even among affected members of …

DiGeorge syndrome (DGS) is one of a group of phenotypically similar disorders, including velocardiofacial syndrome (VCFS, or Shprintzen syndrome) and conotruncal anomaly face …

In children with this syndrome, a tiny piece of one of the copies of chromosome 22 is missing. This can cause many health problems. These problems may range from heart defects and …

22q11.2 deletion syndrome (22q11.2DS), also known as DiGeorge syndrome, is a genetic disorder that occurs when a small piece of one of the baby’s chromosomes – chromosome 22 …