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A diagnosis of Marfan syndrome is made through what process?
GaleEncyofMedicine
The diagnosis is made by taking a family history and a thorough examination of the patient's eyes, heart, and bone structure.
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∙ 13y ago
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The inheritance of Marfan syndrome is an example of?
The "autosomal dominant" method of inheritance. if your question as Marfan syndrome is the result of inheriting a single allele. Individuals with Marfan syndrome are tall and long-limbed, and have both cardiovascular and eye defects. The inheritance of Marfan syndrome is an example of ______. then the answer is pleiotropy
The inheritance of Marfan syndrome is an example of what?
Pleiotropy.
What is the inheritance of marfan syndrome is an example of?
Pleiotropy.
What is an inherited syndrome marked by a tall thin body with arachnodactyly?
Marfan syndrome
Is gene therapy a possiblilty for marfan's syndrome?
Unfortunately no. The mutation that causes Marfan syndrome is found in every single cell in the body. It would be impossible to replace it in every cell.
Why is a diagnosis of Marfan syndrome easier to make in adults than in children?
Most of the external features of Marfan syndrome become more pronounced as the patient gets older, so that diagnosis of the disorder is often easier in adults than in children.
Why is rapid genetic diagnosis impossible in cases of Marfan syndrome?
Mutations of the fibrillin gene (FBNI) are unique to each family affected by Marfan, which makes rapid genetic diagnosis impossible, given present technology.
Why are dislocated lenses an indication of Marfan syndrome?
This condition is an important indication for diagnosis of the syndrome because there are relatively few other disorders that produce it.
What is the life expectincy of marfan syndrome?
With proper treatment (medications, regular checks of the aorta, preventative surgery), a person with Marfan syndrome has an average life expectancy into their mid 70s. If a person does not know they have the diagnosis or does not do proper care, the life expectancy can be the 40s. This is why proper diagnosis is key!
What are the chances of getting marfan syndrome?
Marfan syndrome is found in 1 in every 5,000 - 10,000 births. If one of your parents has Marfan syndrome, you have a 50% chance of having Marfan syndrome.
Is marfan syndrome automsomal dominant?
Yes, Marfan syndrome is autosomal dominant.
What does Marfan syndrome mean?
Marfan Syndrome is a medical problem with the Conective Tissue.
Is Marfan syndrome contagious?
Marfan's syndrome is not contagious. A person can only get it by inheriting it from a parent.
Is Down Syndrome the same as Marfan Syndrome?
No. Down is caused by an extra chromosome while Marfan is due to a mutation in one or more genes.
Why is it sometimes impossible to make a conclusive diagnosis of Marfan syndrome?
The diagnosis remains uncertain because of the mildness of the patient's symptoms, the absence of a family history of the syndrome, and other variables. These borderline conditions are sometimes referred to as marfanoid syndromes.
How does a person inherit marfan syndrome?
Marfan syndrome is an inherited disorder that is typically passed down from one generation to the next through an autosomal dominant pattern of inheritance. This means that if one parent carries the Marfan syndrome gene, there is a 50% chance that they will pass it on to each of their children. In some cases, Marfan syndrome may also occur as a result of a spontaneous genetic mutation.
The inheritance of Marfan syndrome is an example of?
The "autosomal dominant" method of inheritance. if your question as Marfan syndrome is the result of inheriting a single allele. Individuals with Marfan syndrome are tall and long-limbed, and have both cardiovascular and eye defects. The inheritance of Marfan syndrome is an example of ______. then the answer is pleiotropy
