0
Goldenhar syndrome is not an inherited syndrome, it is just in a persons genes and there is no way to stop a baby from getting it in the womb. Goldenhar syndrome is not developed or passed on to the foetus it is just there.
hope this helped you as i am a sufferer of goldenhar syndrome myself! :)
Wiki User
∙ 12y ago
Add your answer:
Earn +20 pts
What is short person syndrome?
Usually called, "Napoleon Syndrome" since Napoleon was very short in stature.
Why does an individual with Turners syndrome often NOT get diagnosed till adolescence?
Sometimes the person does not have obvious characteristics of Turner syndrome, so they do not get diagnosed as a child. When they become adolescent and do not go through puberty that is what leads the doctor to test the person for Turner syndrome.
Is it true that a person who inherits two X chromosomes will be a male?
Answer:This is not true. If you inherit two X chromosomes you will be a girl. A boy has a X and a Y chromosome. I don't know for sure, but I think so. After all, the numbers xs are greater than ysAnswer:No, it isn't. A person with XY chromosomes is male. Two X chromosomes is female.Answer:It is possible but they have to inherit a Y chromosomes. It called Klinefelter's syndrome (KS). KS has two X chromosomes and one Y chromosome. They can grow breast and have an ovary and have anger problems. Most men like this in up in prison.
What are the scenarios of passing turner syndrome?
It is not passed on from parent to child. It is an error in meiosis.
The most common autosomal abnormality is seen is a person with?
Down syndrome
What cause Goldenhar Syndrome?
causes are Multifactorial but there may be due to gentic component
When did Maurice Goldenhar die?
Maurice Goldenhar died in 2001.
When was Maurice Goldenhar born?
Maurice Goldenhar was born in 1924.
How can Goldenhar Syndrome affect a persons life?
Oculo-Auriculo Vertebral Syndrome-is rere congenital defect characterised by incomplete development of ear ,nose,soft palte & mandibles
How is Williams syndrome carried on?
if you were born and your mother or father had William syndrome, you can inherit the syndrome or disease.
How it is possible to have klinefelter syndrome?
One must surly inherit it from their parents.
If you have Andersen's syndrome what are the chances that your two children will have it?
Andersen's syndrome is usually inherited in an autosomal dominant fashion. This means that EACH child of a person with Andersen's syndrome will have a 50% chance of inheriting the gene associated with the syndrome. However, not all people who inherit the gene will show symptoms of the syndrome. Children of people affected with Andersen's syndrome should be evaluated by a qualified physician to determine risk.
Where did down syndrome come from?
Downs syndrome is a genetic abnormality caused by an extra chromosome, in simple terms - as a healthy individual you inherit 22 chromosomes from your mother and 22 from your father, so that's 44 altogether, 1 chromosome from each of your parents will combine to form 22 sets, in a person with Downs syndrome there is an extra abnormally shaped set of chromosomes. So in short a person with Downs syndrome has 23 chromosomes instead of 22.
Is Marfan's symdrome a transmitted disease?
Marfan's syndrome is a genetic disorder, so one would inherit it from their biological parents. You can't "catch" marfans syndrome
Can a person with felony inherit a house?
of course
Do you inherit high blood presssure?
A person does not technically inherit high blood pressure, but a person can inherit the tendency to develop high blood pressure. As well, personal habits combine to cause a tendency to become a reality.
Is Marfan Syndrome common in a specific race?
About 1 in 5,000 people have Marfan syndrome, including men and women of all races and ethnic groups. About 3 out of 4 people with Marfan syndrome inherit it, meaning they get the genetic mutation from a parent who has it. But some people with Marfan syndrome are the first in their family to have it; when this happens it is called a spontaneous mutation. There is a 50 percent chance that a person with Marfan syndrome will pass along the genetic mutation each time they have a child.
