Information about your child
Source: NHS
In this topic (6)
If your child hasEdwards' syndrome, your clinical team will pass information about him or her on to the National Congenital Anomaly and Rare Diseases Registration Service (NCARDRS).
This helps scientists look for better ways to prevent and treat this condition. You can opt out of the register at any time.
Edwards' syndrome is rarely inherited and the condition is not caused by anything the parents have done. The development of three copies of chromosome 18 usually happens randomly during the formation
If your child hasEdwards' syndrome, your clinical team will pass information about him or her on to the National Congenital Anomaly and Rare Diseases Registration Service (NCARDRS). This helps scient
Edwards' syndrome, also known as trisomy 18, is a serious genetic condition caused by an additional copy of chromosome 18 in some or all of the cells in the body.
Pregnant women are offered screening for Edwards syndrome between 10 and 14 weeks of pregnancy to assess the chances of their baby having the condition. The screening test, known as the combined test
There are two main types of Edwards' syndrome. Full form Approximately 94% of babies with Edwards' syndrome will have thefull form, where every cell in their body has three copies of chromosome 18,
Babies with Edwards' syndrome can have a wide range of different problems. Physical signs of Edwards' syndrome include: a small, abnormally shaped head a small jaw and mouth long fingers that ove
