Yes it is, the mutation lies on chromosome 15. This carries the code for the structure of fibrillin which is an important part of collagen, the main component of connective tissue.
Chromosomal abnormality is a broader term, describing duplications, loss, gain etc, of a particular chromosome. More related to the structures in an ideogram.Genetic disorder is a much broader term that describes any chromosomal or genetic changes. A disease condition.
It is not passed on from parent to child. It is an error in meiosis.
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
Pleiotropy.
Pleiotropy.
Yes
Yes. Marfan syndrome is caused by a defect (or mutation) in the gene that tells the body how to make fibrillin-1.
no, it is a chromosomal abnormality, not a contagious disease.
There are many different chromosomal abnormalities in a RETT patient it includes ring chromosome(especially X chromosome),dicentric,chromosomal and chromatid breaks etc...
It is called Patau syndrome and is a chromosomal abnormality
Trisomy 21, Down's syndrome
46,XXY or XXY for males; see the link below.
If one of sex chromosomes is missing. Normal-XX Turner- XO
what is the answer to this question
Chromosomal abnormality is a broader term, describing duplications, loss, gain etc, of a particular chromosome. More related to the structures in an ideogram.Genetic disorder is a much broader term that describes any chromosomal or genetic changes. A disease condition.
It is the result of a chromosomal abnormality, in which there is an extra chromsome on the chromosome 21 pair. This is call trisomy 21.
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.