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What is the technique used to detect genetic disorders by the removal of a small amount of the amniotic fluids?

The technique used to detect genetic disorders by removing a small amount of amniotic fluid is called amniocentesis. This procedure involves inserting a needle into the amniotic sac surrounding the fetus to collect a sample of amniotic fluid, which contains fetal cells for genetic testing. Amniocentesis is typically performed during the second trimester of pregnancy to assess the risk of chromosomal abnormalities or genetic disorders in the fetus.


Can Russell Silver Syndrome be caused by lack of fluid around the baby?

My son has Russell-Silver Syndrome....It has NOTHING to do with the amount of fluid around the baby. It is a form a Primordial Dwarfism, meaning, that the baby was conceived that way. It is definitely something genetic, but it's exact genetic cause or marker is not yet known.


How can amniocentesis detect a disorder like Down syndrome?

Amniocentesis involves testing a sample of amniotic fluid surrounding the fetus to examine the fetal cells for genetic abnormalities. In the case of Down syndrome, amniocentesis can identify the presence of an extra copy of chromosome 21 in the fetal cells, which is characteristic of the disorder. This test can provide information about the genetic makeup of the fetus and help diagnose Down syndrome.


Name two genetic disorders?

Two genetic disorders are Turner's syndrome and cystic fibrosis.


What are the genetic disorder caused by deletion from chromosome?

Deletion Syndrome or Williams Syndrome

Related Questions

Can amniotic band syndrome lead to amputation?

Yes it can. It can also be fatal.


Can amniotic band syndrome be cured?

No, there is no way to know that a fetus has amniotic band syndrome until they are born. Once the baby is born, they will have a treatment plan tailored just for them since no 2 cases of this are ever the same.


What can cause low amniotic fluid?

Low amniotic syndrome usually an indication of downs syndrome.


What fetal defects can be detected from amniotic fluid?

malnourished,uncompleted body parts,not improved senses of organ.


Is Asperger's Syndrome behavioral or genetic?

It is genetic.


What is the technique used to detect genetic disorders by the removal of a small amount of the amniotic fluids?

The technique used to detect genetic disorders by removing a small amount of amniotic fluid is called amniocentesis. This procedure involves inserting a needle into the amniotic sac surrounding the fetus to collect a sample of amniotic fluid, which contains fetal cells for genetic testing. Amniocentesis is typically performed during the second trimester of pregnancy to assess the risk of chromosomal abnormalities or genetic disorders in the fetus.


When can you get marfan syndrome?

Anyone can get Marfans syndrome, it is a genetic disorder.


What important genetic characteristic does Marfan syndrome have?

Another important genetic characteristic of Marfan syndrome is variable expression.


Synonym for duplication syndrome?

What specific genetic syndrome are you referring to? - for there are quite a few genetic syndromes, secondary to chromosomal duplication.


Is down syndrome constitutional?

is down syndrome acquired genetic disease


Is marfan syndrome genetic?

yes


Is klinefelter's syndrome genetic?

yes