One can find information on marfan on its official website. Marfan syndrome is a disorder that affects connective tissue. It is usually passed from parent to child through genes.
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.
It is unsure, whether he did or did not. There is too little information from him, to find out exactly. Chances are he did not, and had some other disease.
you get it from one gene from your family
Marfan syndrome is one of the more common inheritable disorders.
Support groups are often good sources of information about Marfan; they can offer helpful suggestions about living with it as well as emotional support.
a change in one chromosone
A few patients with Marfan may have a pectus excavatum on one side of their chest and a pectus carinatum on the other.
No. Down is caused by an extra chromosome while Marfan is due to a mutation in one or more genes.
It is estimated that one person in every 3000-5000 has Marfan syndrome, or about 50,000 people in the United States.
Marfan disease was found in 1896, by a French doctor named Antione B. Marfan
The medical terminology for the condition is pectus excavatum. It is a common characteristic of people who have Marfan's Syndrome, and their website probably has the most detailed account on all the factors involved.
Antoine Marfan was born in 1858.