Special needs pregnancy - special tests can detect early fetal defects.

Post your message here Decrease your exam stress by using our latest Testking 640-461 guide and best quality Testking 642-832 guide. Although questions provide with 100% pass guarantee along with Testking 70-646 questions guide. Further want to share about unique military jacket along with great choice of cheap coats.

Pregnancy books tend to gloss over special needs pregnancy and prenatal classes frequently choose to ignore the possibility that you might give birth a baby with special needs.

Depending on a mother's risk profile, special tests may be ordered to detect early fetal birth defects.

Ultrasound

Ultrasound utilizes sound waves that bounce off tissues. These waves of sound are deflected and converted into images of the fetus, which then appear on a screen.

Ultrasound detects the number of fetuses, age and growth rate of the fetus, location of the placenta, fetal position and heart rate, amount of amniotic fluid in the uterus and some birth defects.

Alpha-Fetoprotein (AFP) Screen

Alpha-fetoprotein (AFP) screening is a blood test used to detect neural tube defects or Down syndrome.

It is performed between weeks 15-18. Every fetus produces alpha-fetoprotein that passes from the amniotic fluid into the mother's blood. If a fetus has an open neural tube defect (spina bifida), excessive quantities of alpha-fetoprotein leak into the mother's blood. Low levels of alpha-fetoprotein are associated with Down syndrome. This test identifies 90 percent of open neural tube defects and 25 percent of Down's cases. False positives occur almost 5 percent of the time.

Amniocentesis

With amniocentesis, fetal cells present in the amniotic fluid are collected from a needle inserted into the abdomen. These cells are then cultured and grown in order to detect chromosomal abnormalities, including Down syndrome. The test is performed between 14 - 18 weeks.

Chorionic Villus Sampling

Chorionic villi are microscopic projections that compose the placenta. They have the same genetic constitution as the fetus. The villi sample is collected either through a needle in the abdomen or through a vaginal catheter and cultured to detect chromosomal abnormalities. This test is performed in the first trimester.

Serum screening

Various versions of this blood test exist as double test or triple test. They are all types of serum screening and differ only slightly from one another. The serum screening test is a blood test offered between 15-20 weeks. It combines the results of AFP test with measurement of other chemicals in your blood to give a risk factor for your baby to be born with Down's syndrome.

As the AFP test results are combined with this, the risk factor works out for spina bifida as well.

Cordocentesis

Cordocentesis is the extraction of a blood sample from the umbilical cord. This test can be carried out late in pregnancy, between 18 to 24 weeks. It is carried out in women who are at a higher risk of chromosomal/genetic abnormalities.

Fetoscopy

A very modern and fairly new procedure, fetoscopy involves extraction of umbilical cord and placental samples to check for certain skin and blood disorders that cannot be detected by amniocentesis. This can be carried out after 16 weeks of pregnancy and carries a 3-5% risk of miscarriage.

Miscarriage

A miscarriage is the loss of a baby before the 20th week of pregnancy. Many losses occur before a woman knows she is pregnant. About 15 percent of recognized pregnancies and as many as 50 percent of all pregnancies end in miscarriage.

Most miscarriages occur in the first trimester (12 weeks) of pregnancy. The causes of miscarriage are not entirely known. The most common reason for first-trimester losses is a chromosomal abnormality in the baby. Infections, hormonal problems and health problems in the mother can also cause a miscarriage.

Chromosomal Abnormalities

About 1 in 150 babies is born with a chromosomal abnormality. These are caused by errors in the number or structure of chromosomes. There are many different chromosomal abnormalities. Many children with a chromosomal abnormality have mental and/or physical birth defects. Understanding what chromosomes are may make it easier to understand the wide range of problems chromosomal abnormalities can cause.

Sometimes a baby can be born with too many or too few chromosomes, or with one or more chromosomes that are missing a piece or are rearranged. These errors in the number or structure of chromosomes can cause a wide variety of birth defects ranging from mild to severe. Some chromosomal abnormalities result in miscarriage or stillbirth.

What causes chromosomal abnormalities?

Chromosomal abnormalities usually result from an error that occurred when an egg or sperm cell was developing. It is not known why these errors occur. As far as we know, nothing that a parent does or doesn't do before or during pregnancy can cause a chromosomal abnormality in his or her child.

But sometimes something goes wrong before fertilization. An egg or sperm cell may divide incorrectly, resulting in an egg or sperm cell with too many or too few chromosomes. When this cell with the wrong number of chromosomes joins with a normal egg or sperm cell, the resulting embryo has a chromosomal abnormality. A common type of chromosomal abnormality is called a trisomy. This means that an individual has three copies, instead of two, of a specific chromosome.

Down syndrome is an example of a trisomy. Individuals with Down syndrome generally have three copies of chromosome 21. Children with Down syndrome have varying degrees of mental retardation, characteristic facial features and, often, heart defects and other problems.The risk of Down syndrome and other trisomies increases with maternal age.

In most cases, an embryo with the wrong number of chromosomes does not survive. In such cases, the pregnant woman has a miscarriage. This often happens very early in pregnancy, before a woman may realize she's pregnant. Up to 75 percent of first trimester miscarriages are caused by chromosomal abnormalities in the embryo.

Other errors also can occur, usually before fertilization. These errors can alter the structure of one or more chromosomes. Individuals with structural chromosomal abnormalities usually have the normal number of chromosomes. However, small pieces of a chromosome (or chromosomes) may be deleted, duplicated, inverted, misplaced or exchanged with part of another chromosome. These structural rearrangements sometimes have no effect, if all of the chromosome is there but just rearranged, or it may result in pregnancy loss or birth defects.

Errors in cell division also can occur soon after fertilization. This can result in mosaicism, a condition in which an individual has cells with different genetic makeups. For example, individuals with the mosaic form of Turner syndrome are missing an X chromosome in some, but not all, of their cells. Some individuals with chromosomal mosaicism may be mildly affected, but the severity of the condition depends largely on the percentage of abnormal cells.

How are chromosomal abnormalities diagnosed?

Chromosomal abnormalities can be diagnosed after birth using a blood test, or before birth using prenatal tests (amniocentesis or chorionic villus sampling). Cells obtained from these tests are grown in the laboratory, and then their chromosomes are examined under a microscope. The lab makes a picture (karyotype) of all the person's chromosomes, arranged in order from largest to smallest. The karyotype shows the number, size and shape of the chromosomes and helps experts identify any abnormalities.

What are the most common chromosomal abnormalities?

Down syndrome is one of the most common chromosomal abnormalities, affecting about 1 in 800 babies. The risk of Down syndrome and other trisomies increases with the mother's age.

The outlook for children with Down syndrome is far brighter than it once was. Most have mental retardation in the mild to moderate range. With early intervention and special education, many learn to read and write and participate in diverse childhood activities.

Babies also can be born with an extra copy of chromosome 13 or 18. These trisomies are usually more severe than Down syndrome, but fortunately less common. About 1 in 10,000 babies is born with trisomy 13 (also called Patau syndrome), and about 1 in 6,000 with trisomy 18 (also called Edwards syndrome) (3, 6). Babies with trisomies 13 or 18 generally have severe mental retardation and many physical birth defects. Most affected babies die before their first birthday.

The X and Y chromosomes are referred to as sex chromosomes. About 1 in 500 babies has missing or extra sex chromosomes. Generally, females have two X chromosomes, and males have one X chromosome and one Y chromosome. Sex chromosome abnormalities may cause infertility, growth abnormalities, and in some cases, behavioral and learning problems. However, most affected individuals live fairly normal lives.

Turner syndrome is a sex chromosome abnormality that affects about 1 in 2,500 girls. Girls with Turner syndrome are missing all or part of one X chromosome. They usually are infertile and do not undergo normal pubertal changes unless they are treated with sex hormones. Affected girls are short, though treatment with growth hormones can help increase height. Some have other health problems, including heart and kidney defects. Girls with Turner syndrome generally have normal intelligence, though some have difficulties with mathematics and spatial concepts.

About 1 in 1,000 females has an extra X chromosome, referred to as triple X. Affected girls tend to be tall. They usually have no physical birth defects, undergo normal puberty and are fertile. Affected girls usually have normal intelligence, though many have learning disabilities. Because these girls are healthy and have a normal appearance, their parents often don't know they have a chromosomal abnormality. Some parents may learn that their daughter has this abnormality if they have prenatal testing (with amniocentesis or chorionic villus sampling).

Klinefelter syndrome is a sex-chromosome abnormality that affects about 1 in 500 to 1,000 boys (3, 4) Boys with Klinefelter syndrome have two, or occasionally more, X chromosomes along with their Y chromosome (males normally have one X and one Y chromosome). Affected boys usually have normal intelligence, though many have learning disabilities. As adults, they produce lower-than-normal amounts of the male hormone testosterone (and often are treated with this hormone) and are infertile.

About 1 in 1,000 males is born with one or more extra Y chromosomes (3). Affected males are sometimes taller than average, have normal sexual development and are fertile. Most have normal intelligence, though some have learning disabilities, and behavioral and speech/language problems. As with triple X females, many affected males and their families don't know they have a chromosomal abnormality unless it is diagnosed with prenatal testing.

Are there other, less common, chromosomal abnormalities?

New techniques for analyzing chromosomes have made it possible to identify tiny chromosomal abnormalities that may not be visible even under a high-powered microscope. As a result, more parents are learning that their child has a chromosomal abnormality. Some of these uncommon chromosomal abnormalities include:

* Deletion: A small section is missing.
* Microdeletion: A minute amount of material (sometimes only a single gene) is missing.
* Translocation: A section of a chromosome is attached to another chromosome.
* Inversion: A section of chromosome is snipped out and reinserted upside down.
* Duplication: A section of a chromosome is duplicated, so there is extra genetic material.
* Ring chromosome: Material is deleted at both ends of a chromosome, and the new ends join together to form a ring.

Some of these abnormalities are so rare that only one or a few children are known to be affected. In such cases, it may be impossible for a doctor to predict a child's long-term health and development. Some abnormalities (such as some translocations and inversions) may not affect a person's health if no genetic material is missing or duplicated.

Some rare disorders can be caused by small chromosomal deletions. Some examples are:

* Prader-Willi syndrome (deletion on chromosome 15): Affected children usually have mental retardation or learning disabilities, behavioral problems and short stature. They also may develop extreme obesity.

* Cri-du-chat (cat cry) syndrome (deletion on chromosome 5): Affected children have a cat-like high-pitched cry during infancy, mental retardation and physical abnormalities.

* Wolf-Hirschhorn syndrome (deletion on chromosome 4): This disorder is characterized by severe mental retardation, heart defects, poor muscle tone, seizures, high blood pressure and other problems.

* 22q11 deletion syndrome (deletion on chromosome 22): Deletions in a specific region of chromosome 22 cause a variety of problems that can include heart defects, cleft lip/palate, immune system abnormalities, characteristic facial features and learning disabilities. Certain combinations of these features are sometimes called DiGeorge or velocardiofacial syndrome. Individuals with this disorder have a 50 percent chance of passing the chromosomal abnormality on to their offspring with each pregnancy.

With the exception of individuals with 22q11 deletion syndrome, individuals with these disorders generally do not reproduce.

Are all children with the same chromosomal abnormality alike?

No. Each child with a chromosomal abnormality should be evaluated as an individual. Even parents with apparently identical chromosomal abnormalities can differ substantially from each other. How a person is affected depends greatly, but not wholly, on the exact genetic material involved. Each chromosome contains hundreds to thousands of genes, and each gene influences different characteristics or body functions.

New techniques of analyzing chromosomes sometimes can pinpoint exactly where missing or extra genetic material comes from. If doctors know what genes are contained in that section and their function, they sometimes can give parents a better prediction of a child's future development.

Will the brothers and sisters of a child with a chromosomal abnormality have the same problem?

Parents who have had a baby with a chromosomal abnormality should consult a genetic counselor. These health professionals help families understand what is known about the causes of a birth defect, and the chances that the birth defect will recur in another pregnancy. Fortunately, in most cases, parents of a baby with a chromosomal abnormality learn that the risk is low. For example, parents of a baby with Down syndrome usually have about a 1 percent risk of having another affected baby, if the mother is under age 35. Mothers over age 35 are believed to have a risk similar to other women their age.

However, there are exceptions. For example, a small number of parents of children with Down syndrome or various other chromosomal abnormalities have a chromosomal rearrangement (balanced translocation) that does not affect their own health. However, these rearrangements can be harmful when passed on to their offspring. Sometimes a genetic counselor recommends blood tests to determine whether parents carry such a rearrangement in order to give the parents the most accurate picture of their risk in another pregnancy. Testing also may occasionally show that a parent of a child with 22q11 deletion syndrome has a mild, previously undiagnosed form of the disorder that can be passed along to future offspring.

Where can families affected by chromosomal abnormalities turn for help?

An affected baby's doctor should be able to discuss specific medical problems in detail or refer a family to appropriate specialists. Parents also may find it helpful to contact a support group made up of families of children affected by the same or similar chromosomal abnormalities. A genetic counselor is a good source of referrals to appropriate support groups. Some of them include:

Most women who have an early miscarriage do not need treatment. The uterus empties itself. Sometimes, the woman's health care provider recommends a procedure called a Dilation and curettage - D&C.

Almost all women go on to have a healthy pregnancy after a miscarriage. Some women have repeated miscarriages. Still, about 60 to 70 percent of those who have had two or three losses go on to have a healthy pregnancy.

What you can do:

Report any bleeding or abdominal pain to your health care provider. She or he may do an internal exam and an ultrasound to check the baby.

If you do have a miscarriage, give yourself time to recover physically and to grieve the loss of your baby. If you have repeated miscarriages, ask your health care provider to help you find their cause. Testing reveals the cause of the miscarriages in up to 50% of couples.

Additional special needs pregnancy resources