Translocation 21;21 / Robertsonian Translocation

I get a lot of hits on my blog on the following topics:

Translocation Down syndrome
Translocation 21;21
Translocation Carrier
Trisomy 21 Translocation
Karyotype trisomy 21 translocation
Translocation 21 Trisomy

As Translocation 21;21 is very rare, and a lot of people seem to be googling this, I decided to set up a yahoo mail group for parents, families, friends, individuals, experts with Translocation 21,21 experience who wants to share their experience/learn more about Translocation 21;21.

If you are interested to join send me an email at cmolin77[at]hotmail.com or click here!

If you want to see what a Translocation 21;21 kariyotype looks like, click here.
In short, if you are a carrier of T21;21 there is a 100% chance of all your babies having DS. There is no other way with this type of Translocation.

From the following web page you can read about T21,T21  and it is a little more descriptive of what Translocational T21/DS really is:

Translocation Down syndrome refers to the rearranged chromosome material. There are three # 21 chromosomes, just like there are in trisomy 21, but one of the 21 chromosomes is attached to another chromosome, instead of being separate. The extra # 21 chromosome is what causes the problems that make up Down syndrome. In translocation Down syndrome, the extra 21 chromosome may be attached to the #14 chromosome, or to #s13, 15, or 22. In some cases, two #21 chromosomes can be attached to each other.

Three to 4 percent of babies born with Down syndrome have translocation Down syndrome. If you had a roomful of 100 babies with Down syndrome, they would all look alike and have similar features and health problems. You would not be able to pick out the three or four that have a translocation.

Whenever a translocation is found in a child, the parents’ chromosomes are studied to determine whether the translocation was inherited or not. If one parent has the translocation chromosome, then the physician knows the baby inherited the translocation from that parent. The parent will actually have 45 total chromosomes in each cell of their body, but they will be normal and healthy because they still have only two copies of each chromosome. When a person has a rearrangement of chromosome material, with no extra or missing chromosome material, they are said to have a “balanced translocation” or be a “balanced translocation carrier.”

Parents with balanced translocations may have fertility problems (trouble becoming pregnant), miscarriages, or have an increased chance of having a child with health problems. Although the parent can donate the proper amount of genetic material (23 chromosomes) to a pregnancy, they have a risk of donating too much or too little genetic material to a pregnancy. It is not something they can control or predict. The chance depends on the type of chromosome rearrangement and which chromosomes are involved. For example, if the translocation is between #14 and 21, there is a 10 to 15 percent chance for Down syndrome in a pregnancy if the mother is the translocation carrier, and a 3 to 5 percent chance if the father is the translocation carrier. The chances are different for men and women because sperm and eggs are produced differently. A woman is born with all of the eggs she will ever have while men are constantly producing new sperm.

There is another important factor to remember when a parent is found to have a translocation. The parents’ relatives (brothers, sisters) may also have inherited the translocation and, therefore, may have the same risks for problems with a pregnancy. For these reasons, it is recommended that people with chromosome rearrangements share this information with their relatives so that they can have the option of having their chromosomes studied.