Down's Syndrome and Nuchal Translucency Scans | 4D Baby Scan
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Down with Down's Syndrome
Ask a pregnant mother what sex she prefers her baby to be, what names she's planned to give the baby and she will giddily respond. Ask her, however, whether she plans to try and go for those nuchal scans and you will be looked at as a lunatic eager to burst her bubble.
The occurrence of potential birth defects is the elephant in the room of expecting parents. It is something nobody likes to even consider, but nuchal scans and other tests that could detect anomalies early is a good option for all pregnancies.
This nuchal screening test detects the presence of hormones that tend to be higher when the woman could be carrying a baby with Down's. Nuchal scan ultrasounds distinguish these anomalies before you give birth, administered from the 11th to 13th week of pregnancy: in the first trimester of pregnancy. This specific blood test or a serum biochemistry test may be given to a mother who has a predisposition to having a baby with Down's Syndrome.
Most definitely not something that conjures happy thoughts, these scans and other assessments do a lot to help you manage a potential problem. During the first three months into your pregnancy, mothers who are at higher risk of having a baby with Down's syndrome are given this serum biochemistry.
What they are are attempting to detect is what is known as translucency, the measure of fluid in the area behind the neck.
This particular translucency itself is not what is indicative of the anomaly, but the presence of abnormally elevated amounts is a cause for concern.
Time is of the essence in this particular scan. If and when you miss this window, there is no more chance to make it work. There will be no other way to distinguish it. The fluid that is measured dissipates on its own after this window.
If you have a predisposition to having a baby with Down's if you got pregnant late, or if you've had a suggestive result on another anomaly testing, you should definitely go for it. You become at higher risk for Down's as you get older. The Nuchal scan is tremendously accurate. Your doctor might have other tests done in tandem for good measure. Again, I will need to reiterate: the accuracy and the scan's ability to distinguish issues relies almost completely on your timing.
Working with your healthcare professional and prenatal care provider closely can help eliminate this error. If you set and meet appointments with them regularly, they will ensure that you make it to every pregnancy scan exactly when you need it. Don't scrimp on finding a reputable clinic and a good doctor for this challenging period!
No expectant mother likes to entertain the thought of their baby not being as perfect as they want, but nuchal scans help prepare you and eliminate the unknown by monitoring and detecting possible anomalies. Work with your doctor if you feel you could be at risk. Work with your doctor, I've said it before and I'm not ashamed to sound redundant here, because of how important it really is.
Another relevant topic is how 4d baby scan can strengthen maternal bonding.
The occurrence of potential birth defects is the elephant in the room of expecting parents. It is something nobody likes to even consider, but nuchal scans and other tests that could detect anomalies early is a good option for all pregnancies.
This nuchal screening test detects the presence of hormones that tend to be higher when the woman could be carrying a baby with Down's. Nuchal scan ultrasounds distinguish these anomalies before you give birth, administered from the 11th to 13th week of pregnancy: in the first trimester of pregnancy. This specific blood test or a serum biochemistry test may be given to a mother who has a predisposition to having a baby with Down's Syndrome.
Most definitely not something that conjures happy thoughts, these scans and other assessments do a lot to help you manage a potential problem. During the first three months into your pregnancy, mothers who are at higher risk of having a baby with Down's syndrome are given this serum biochemistry.
What they are are attempting to detect is what is known as translucency, the measure of fluid in the area behind the neck.
This particular translucency itself is not what is indicative of the anomaly, but the presence of abnormally elevated amounts is a cause for concern.
Time is of the essence in this particular scan. If and when you miss this window, there is no more chance to make it work. There will be no other way to distinguish it. The fluid that is measured dissipates on its own after this window.
If you have a predisposition to having a baby with Down's if you got pregnant late, or if you've had a suggestive result on another anomaly testing, you should definitely go for it. You become at higher risk for Down's as you get older. The Nuchal scan is tremendously accurate. Your doctor might have other tests done in tandem for good measure. Again, I will need to reiterate: the accuracy and the scan's ability to distinguish issues relies almost completely on your timing.
Working with your healthcare professional and prenatal care provider closely can help eliminate this error. If you set and meet appointments with them regularly, they will ensure that you make it to every pregnancy scan exactly when you need it. Don't scrimp on finding a reputable clinic and a good doctor for this challenging period!
No expectant mother likes to entertain the thought of their baby not being as perfect as they want, but nuchal scans help prepare you and eliminate the unknown by monitoring and detecting possible anomalies. Work with your doctor if you feel you could be at risk. Work with your doctor, I've said it before and I'm not ashamed to sound redundant here, because of how important it really is.
Another relevant topic is how 4d baby scan can strengthen maternal bonding.
Down's Syndrome Screening Made Safe and Simple
(also known as Downs Syndrome or Down Syndrome)
Down's Syndrome Screening Made Safe and Simple (also known as Downs Syndrome or Down Syndrome)
Down Syndrome is a genetic chromosomal disorder seen in babies born with aberrations of chromosome 21. Normal individuals, you and I, are born with a total of 46 chromosomes including the sex chromosomes. Each pair of chromosomes is given a number except the sex chromosomes which are called XX or XY.
How Does Downs Occur?
The process of inheritance and passage of chromosomes from parents to offspring is complex, but to put the matter simply, each parent passes a half a chromosome (in other words, a strand) to the offspring. A matched strand from each parent pair up to form a complete chromosome for the offspring. Genetic material carried in each chromosome is responsible for a specific set of features and processes, such as eye colour or gender.
The disorder in Down's Syndrome, technically known as Trisomy 21, occurs as a result of 3 strands of chromosome 21 being in a child (instead of a single pair or two strands).
The extra chromosomal material in Down's Syndrome in the affected baby causes the physical, neurological and physiological features and problems seen when the baby is born.
Typically, the baby has specific facial features including slanted eyes, low set ears, small flat nose and large protruding tongue. The main concerns for many parents and governments are about specific mental disabilities of varying severity.
Read more on Nuchal Scan and Down's Syndrome.
Down Syndrome is a genetic chromosomal disorder seen in babies born with aberrations of chromosome 21. Normal individuals, you and I, are born with a total of 46 chromosomes including the sex chromosomes. Each pair of chromosomes is given a number except the sex chromosomes which are called XX or XY.
How Does Downs Occur?
The process of inheritance and passage of chromosomes from parents to offspring is complex, but to put the matter simply, each parent passes a half a chromosome (in other words, a strand) to the offspring. A matched strand from each parent pair up to form a complete chromosome for the offspring. Genetic material carried in each chromosome is responsible for a specific set of features and processes, such as eye colour or gender.
The disorder in Down's Syndrome, technically known as Trisomy 21, occurs as a result of 3 strands of chromosome 21 being in a child (instead of a single pair or two strands).
The extra chromosomal material in Down's Syndrome in the affected baby causes the physical, neurological and physiological features and problems seen when the baby is born.
Typically, the baby has specific facial features including slanted eyes, low set ears, small flat nose and large protruding tongue. The main concerns for many parents and governments are about specific mental disabilities of varying severity.
Read more on Nuchal Scan and Down's Syndrome.
Information on Baby and Child's Health
by healthconscious
Hi to new moms out there! I have written some notes you need to jot down in preparation for the coming of your baby and how to bond with your baby!... more »
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