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DiGeorge syndrome (22q11. 2 deletion syndrome) - Mayo Clinic 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 systems to develop poorly
What Is DiGeorge Syndrome (22q11. 2 Deletion Syndrome)? 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 different areas of your child’s body
22q11. 2 Deletion Syndrome (DiGeorge Syndrome) - Boston Childrens Hospital 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 in caring for children who have 22q11 2 deletion
DIGEORGE SYNDROME - Kennedy Krieger Institute E What is it? DiGeorge Syndrome (DGS) is a particular group of clinical features that frequently occur together as a result of a chro osomal 22 defect The term “22q11 2 deletion syndrome” is commonly used DGS is the most common micro-deletion syndrome, causing poor development of sev
22q11. 2 deletion syndrome: MedlinePlus Genetics 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 the same family
DiGeorge Syndrome - Developmental and Behavioral Pediatrics - Golisano . . . 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 developmental delays to seizures The child may also have changes in how the eyes, nose, or ears look
DiGeorge Syndrome: Background, Classification, Epidemiology DiGeorge syndrome (DGS) is one of a group of phenotypically similar disorders, including velocardiofacial syndrome (VCFS, or Shprintzen syndrome) and conotruncal anomaly face (CTAF) syndrome,