What are the facial features of DiGeorge syndrome?

In some cases people with DiGeorge syndrome have no symptoms at all. Sometimes they have distinctive facial features including hooded eyelids, cheek flatness, a prominent bulbous nasal tip, an underdeveloped chin, or ears that appear prominent with attached lobes.

What does Velocardiofacial Syndrome look like?

VCFS includes many common features: cleft palate, heart defects and a characteristic facial appearance. Other common findings include minor learning problems and speech and feeding problems. Velocardiofacial syndrome is the most common syndrome associated with a cleft palate.

Some of the characteristic facial features are hypertelorism (wide-set eyes), down-slanting eyes, low-set auricles (portion of the ears), prominent nose with squared nasal root, and micrognathia (small size of the lower jaw). Children with DGS can be uninhibited and impulsive, yet they are often very affectionate and able to function socially.

What happens to the heart with DiGeorge syndrome?

Cardiac issues – It affects the aortic chamber of the heart. People with DiGeorge syndrome have a mild heart defect. abnormalities of the thymus gland – The thymus gland plays an important role in the development of the immune system.

How big does a child with DiGeorge syndrome get?

Smaller, more frequent feedings may help; however, the child will probably always be small for his/her age. Children with DGS usually fall between the second and twenty-fifth percentile in size. Learning disabilities may become apparent when a child with DiGeorge enters school.

Can you pass DiGeorge syndrome to your offspring?

If you have a DiGeorge syndrome, there is a 10% chance that you can pass the disease to your offspring. (4, 5, and 6) Facial anomalies – underdeveloped chin, ears rotated back, and big eyelids. Cardiac issues – It affects the aortic chamber of the heart. People with DiGeorge syndrome have a mild heart defect.