What Are The Chances Of Having A Baby With Edwards Syndrome?

by | Last updated on January 24, 2024

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If the screening test shows that the chance of the baby having Down’s syndrome, Edwards’ syndrome or Patau’s syndrome is higher than 1 in 150 – that is, anywhere

between 1 in 2 and 1 in 150

– this is called a higher-chance result.

How common is Edwards syndrome in pregnancy?


About one pregnancy in every 400

is diagnosed with Edwards’ syndrome . However, only one baby in 6,000 is actually born with the condition, because it causes severe developmental problems (Gandhi 2015, Lal 2016).

What increases your chances of having a baby with Edwards syndrome?

Having 3 copies of chromosome 18 usually happens by chance, because of a change in the sperm or egg before a baby is conceived. Your chance of having a baby with Edwards’ syndrome

increases as you get older

, but anyone can have a baby with Edwards’ syndrome.

What are the chances of having a baby with trisomy 18?

Trisomy 18 occurs in

about 1 in 5,000 live-born infants

; it is more common in pregnancy, but many affected fetuses do not survive to term. Although women of all ages can have a child with trisomy 18, the chance of having a child with this condition increases as a woman gets older.

What percentage of babies are born with Edwards syndrome?

Trisomy 18 is the second most common type of trisomy syndrome, after trisomy 21 (Down syndrome).

About 1 in every 5,000 babies

is born with trisomy 18, and most are female. The condition is even more common than that, but many babies with trisomy 18 don’t survive past the second or third trimester of pregnancy.

Does trisomy 18 come from Mom or Dad?

For example, the chance of having a baby with Trisomy 18 is higher in older mothers. In other cases, Trisomy 18 can be inherited due to a familial chromosome rearrangement called a translocation.

Trisomy 18 is never the result of anything a mother or father did

, or didn’t do.

Who is the oldest person with Edwards syndrome?

Someone who knows this only too well is

Michael Fagan

. His daughter, Elaine, was born with Edwards’ syndrome almost 23 years ago. He says she is the longest-living person with the condition in the world.

How long do babies with Edwards syndrome live?

The full form of Edwards’ syndrome is considered to be a life-limiting condition which means it affects how long the baby can live. Around 5 in 10 (52.5%) may live longer than 1 week and around 1 in 10 (12.3%)

may live longer than 5 years

.

What gender does Edwards syndrome affect?

Edward’s syndrome affects

more girls than boys

– around 80 percent of those affected are female. Women older than the age of thirty have a greater risk of bearing a child with the syndrome, although it may also occur with women younger than thirty. Edward’s syndrome was named after Dr. John Edward.

Can ultrasound detect trisomy 18?

Conclusions:

Ultrasound scan for fetal anomalies

is the most effective screening test for trisomy 18. A policy of conservative management for women with positive second-trimester biochemical screening or first-trimester combined screening for trisomy 18 is reasonable in the absence of ultrasound fetal abnormalities.

What happens if my baby has trisomy 18?

Most babies with trisomy 18 have problems that affect all parts of the body.

Heart problems, feeding problems

, and infections are what most often lead to death.

Can I have a normal pregnancy after trisomy 18?

The recurrence risk for a family with a child with full trisomy 18 is usually stated as 1% (1 in 100). Therefore, the vast

majority of parents with an affected fetus or child go on to have normal children

.

Can babies survive trisomy 18?


Fifty per cent of babies born with trisomy 18 survive beyond their first six to nine days

. About 12% of babies born with trisomy 18 survive the first year of life. It is difficult to predict the life expectancy of a baby with trisomy 18 if the baby does not have any immediate life-threatening problems.

How do you know if your baby has Edwards syndrome?

But the only definite way to diagnose Edwards syndrome is

through genetic testing

. This can be done while the baby is in the womb using chorionic villus sampling (CVS) or amniocentesis. Both these tests have a risk of miscarriage. You can talk to your obstetrician or midwife about this.

Who is most likely to get Edwards syndrome?

Edwards’ syndrome occurs in all human populations, but is more prevalent in

female offspring

. A healthy egg and/or sperm cell contains individual chromosomes, each of which contributes to the 23 pairs of chromosomes needed to form a normal cell with a typical human karyotype of 46 chromosomes.

What is high risk for Edwards syndrome?

It is known as the

maternal age-specific risk

or chance and is the background risk or chance of Down syndrome used when interpreting a screening result. As maternal age increases the risk or chance of having a baby with Edwards syndrome or Patau syndrome also increases.

Maria LaPaige
Author
Maria LaPaige
Maria is a parenting expert and mother of three. She has written several books on parenting and child development, and has been featured in various parenting magazines. Maria's practical approach to family life has helped many parents navigate the ups and downs of raising children.