Most children with DiGeorge syndrome grow into adulthood; however, children with severe defects may not survive beyond two to three years.

Survival to ages 40 and 50 years was 89.9% and 73.9%, respectively. Median age at death was 41.5 (range 18.1–68.6) years. Deaths included two (7.7%) of 26 ...

2 deletion syndrome? One to two percent of children born with this syndrome have a life expectancy of two to three years; however, most individuals reach ...

In about 1-2% of cases, some children have a life expectancy of two or three years. Many, however, reach adulthood and have a relatively normal life span.

Probability of survival to age 45 years was approximately 72% for those with major CHD, and 95% for those with no major CHD (p < 0.0001). Conclusion: For adults ...

5 апр. 2019 г. · Probability of survival to age 45 years was approximately 72% for those with major CHD, and 95% for those with no major CHD (p < 0.0001).

Many people with DiGeorge syndrome who reach adulthood will have a relatively normal life span, but ongoing health problems can sometimes mean their life ...

2 With treatment, life expectancy may be normal. Depending on the severity of the disorder, some children will be able to attend regular school and have ...

Long-term outcomes depend on the symptoms present and the severity of the heart and immune system problems. With treatment, life expectancy may be normal.

Most people diagnosed with DiGeorge syndrome have a normal life expectancy with mild symptoms. Severe symptoms can lead to a shortened life expectancy ...