DiGeorge SyndromeEn Español (Spanish Version)
DiGeorge syndrome is a rare genetic disease. It is present at birth. People with complete DiGeorge syndrome have no thymus or parathyroid glands. The thymus plays an important role in the immune system. The parathyroid glands help control calcium in the blood and body.
Thyroid and Parathyroid Glands
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DiGeorge syndrome is caused by a deletion of several genes. The lost genetic material controls the development of the thymus and related glands.
DiGeorge may run in some families but most have no family connection.
Physical features of DiGeorge are present at birth. These features do not worsen with age. They may include:
- Elongated face
- Hooded eyelid
- Small eyes
- Small jaw
- Wide nose
- Small head
- Cleft palate
Other symptoms may include:
- Weak muscles
- Short height
- Tapered and hyperextensible fingers
- Learning difficulties
DiGeorge may also be associated with other health issues such as:
- Immune deficiency leading to increased infections
- Heart defects
- Growth and developmental delays
- Increased incidence of psychiatric disorders
- Hypoparathyroidism—low levels of parathyroid hormone
Occasional abnormalities include structural brain defects,
scoliosis, umbilical or inguinal
hernias, kidney abnormalities, anogenital abnormalities, eye abnormalities, and thyroid problems
Your doctor will ask about symptoms and medical history. A physical exam will be done. If your child has certain heart defects or other DiGeorge related symptoms, genetic tests may be ordered.
Your child's bodily fluids may be tested. This can be done with blood tests.
Images may be taken of your child's bodily structures. This can be done with:
Treatment will be based on the symptoms your child has.
Talk with your doctor about the best treatment plan. Some options include:
Some immune system problems can be severe. They may require immediate treatments.
If the thymus is missing, a thymic tissue transplant may be done. A
bone marrow transplant
may also help boost the immune system. However, there are certain risks for these procedures. The risks will be weighed against the benefits.
Other steps involve monitoring the immune system and treating infections.
Heart defects can impair growth and development.
Certain heart defects may need to be surgically repaired. This repair is often done in the first year of life. Other heart defects will need to be monitored throughout the child's life.
A surgery or series of surgeries may be needed to repair a cleft palate. Your child may also work with a speech therapist. The therapist will help your child with feedings and speech delays.
The missing parathyroid glands can affect the level of calcium in the body and blood. Calcium and vitamin D supplements can help to make up for low parathyroid levels. A low phosphorous diet will also help. Talk to your doctor or a dietitian about changes to your child's diet.
A variety of early intervention therapies may help your child including:
- Speech therapy—to help with feeding problems and speech development
- Occupational therapy—to help with everyday skills an personal care
- Physical therapy—to address physical challenges
- Developmental programs—to help your child reach appropriate developmental milestones
- Psychiatry—to address psychological challenges that may arise. Some may not develop until later in life.
In general, the earlier these therapies start the better the outcomes.
There is no known way to prevent DiGeorge syndrome.
Immune Deficiency Foundation
National Center for Biotechnology Information
Canadian Association of Genetic Counsellors
22q11.2 deletion syndrome. EBSCO DynaMed website. Available at:
Updated March 28, 2010. Accessed August 7, 2013.
DiGeorge syndrome. American Heart Association website. Available at:
Updated April 26, 2011. Accessed August 7, 2013.
DiGeorge syndrome. Lucile Packard Children's Hospital at Stanford website. Available at:
Accessed August 7, 2013.
Last Reviewed August 2013