Yes a karyotype is performed which is a blood test to be able to look at the number of chromosomes a person has, and therefore would be able to identify the extra X chromosome in case someone has it.
A geneticist can diagnose Klinefelter syndrome before your son is born through a fetal cytogenetic analysis.
Parents might decide to have genetic testing to determine if either or both of them carry certain genetic traits that could be passed on to their offspring. Some genetic traits will lead to severe birth defects or problematic diseases that could severely impact the quality of their children's lives. If they are indeed carriers of certain traits, they may choose to avoid having children or choose adoption as an alternative. In this way, they can eliminate their particular genetic line and avoid passing the trait on to the next generation.
you obtain genetic materials from your parents organisms.
Genetic traits are variations of features passed on to offspring from there parents.
This sounds like another way of making reference to biological or bio parents, the man and woman who provided the genetic material that formed you.
Genetics is the study of heredity and the variation in organisms. When studying genetics, you learn about dominant and recessive traits along with much more.
Prader-willi syndrome occurs due to genetic mutation, it is believed that parents with a genetic abnormality, uneffected by the syndrome, pass the mutation to their children. Some studies suggest that the syndrome is due to missing genes in the paternal chromosome, but it may be a combination of both parents.
While Alice in Wonderland Syndrome appears to have some genetic predisposition (as children of sufferers are more likely to suffer as well), it is not always passed to children through their parents.
no if the one of the parents have it and it is genetic then yes. but in this case no because it is not genetic
If you are referring to Ambras Syndrome, also known as Hypertrichosis, it is a genetic defect that gets passed down from parents to their children. So you can't catch it if that is what you were wondering. It causes abnormal hair growth especially on the face.
it is genetic
Down's Syndrome is caused mainly by a mutation in the gene. It is a genetic disorder, which means it was passed on from parents to offspring.
The family members with this have a strange and rare genetic disorder. The children's parents share the same blood. In the Arab culture it is common to marry in your bloodline.The syndrome is known to cause mental retardation and a lack of coordination and balance, which causes the some of the family to have their quadrupedal gait (walking on all fours). Some of the children do not speak.Research proves that the children walk on fours as an adaptation to their genetic condition. Scientists do not offer a cure for Uner Tan syndrome.
The same way any other person is 'made' - by their parents having intercourse ! Down Syndrome is a genetic condition inherited from one or both parents.
Response:There is a genetic component to Asperger's Syndrome. If you have a blood relative with autism or Asperger's Syndrome, you are more likely than average to have a child with autism or Asperger's Syndrome, but it does not mean that you will. If both parents have autism or Asperger's Syndrome, there is an even greater likelihood that they will have children with autism or Asperger's Syndrome, but it does not mean that all or any of their children will. Ongoing research is attempting to determine causes of autism spectrum disorders, but there are still many unanswered questions.I think that there is a strong genetic component to Asperger's Syndrome. Ever since I found that I had it I have begun to notice many of my family members who behave somewhat eccentrically. My father definitely has it. As do most of my relatives on my father's side to some degree or the other.Response:Yes! Asperger's Syndrome is definitely genetic! It's a 50-50 possibility my paternal grandmother had it, because she was "eccentric" herself!Response:There is a strong genetic component as shown in twin studies, but it doesn't necessarily mean that you will inherit it from your parents, or that your children will inherit from you, only that you have a higher likelihood of having AS than the general population if someone in your family has AS or autism.If you have one child with autism or AS, there is an increased chance that a second child will have autism or AS. If you have two children with autism or AS, it is much more likely that your other children will also have autism or AS.
Since Down Syndrome is not genetic and is a trisomy, dominant and recessive genes do not play a role and it is possible for two down syndrome parents to have a child without down syndrome.
Noonan syndrome is caused by the mutation in a particular gene. It is a genetic disorder which means that the child which is born with this disorder, must have been in their parents.
Marfan's syndrome is a genetic disorder, so one would inherit it from their biological parents. You can't "catch" marfans syndrome