answersLogoWhite

0

35 different signs are seen in Marfan syndrome. Most are visible signs associated with the skeletal system. Many grow to above-average height with having long, slender limbs with long fingers and toes. The most deaths involve the cardiovascular system. This gene is dominant. If one parent has it, there is a 50/50 chance that an offspring will have it. Abraham Lincoln was once thought to have had this, but no longer.

User Avatar

Wiki User

12y ago

What else can I help you with?

Continue Learning about Natural Sciences
Related Questions

What trait does Marfan syndrome have?

Auto dominant


Is marfan syndrome automsomal dominant?

Yes, Marfan syndrome is autosomal dominant.


Is marfan syndrome dominant or recessive?

Marfan's Syndrome is inherited in an autosomal dominant pattern. This disease is a disorder that affects the connective tissue in many parts of the body.


Is Marfan Syndrome found on a dominant allele?

Maybe


Is marfan's syndrome sex linked?

Marfan syndrome is not sex linked. It is autosomal dominant and found equally in all genders and ethnicities.


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


Is Cockayne Syndrome a dominant or a recessive trait?

Cockayne syndrome is a recessive trait.


What is the inheritance pattern to Marfan Syndrome?

Marfan syndrome is an autosomal dominant disorder. An affected person has a 50% chance of passing it on to each offspring, regardless of gender.


Marfan syndrome is a genetic disorder caused by a dominant allele. Describe how Marfan syndrome is inherited.?

Marfan syndrome is inherited in an autosomal dominant manner, meaning that only one copy of the mutated gene from an affected parent can lead to the condition in their offspring. If a parent has Marfan syndrome, there is a 50% chance with each pregnancy that the child will inherit the disorder. The gene involved in Marfan syndrome is the FBN1 gene, which affects connective tissue. Both males and females are equally likely to be affected by the disorder.


Dose marfan syndrome have to be on a x chormose?

Marfan syndrome is caused by a mutation in the FBN1 gene, which is located on chromosome 15 and is inherited in an autosomal dominant pattern. It is not linked to the X chromosome. Both males and females can inherit and display symptoms of Marfan syndrome.


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.


Is marfan syndrome x linked?

I think it's dominant because when you have sex you are sharing your love.