Yes he did. Julius Caesar along with Abraham Lincoln were cited in having this syndrome.
Source:King Tut Unwrapped.
Modern research thinks it's doubtful that Caesar had epilepsy. After studying Caesar's symptoms and his lifestyle, the consensus is that he suffered from hypoglycemia, or low blood sugar. The symptoms of low blood sugar mimic those of epilepsy. As the ancients were not familiar with hypoglycemia, but were familiar with epilepsy, they naturally assumed that he was an epileptic.
As of 2014, there are no reported famous people who suffer with Rett syndrome. This condition affects the central nervous system.
Yes it can be, but many women suffer from 1 breast bigger than the other.
Gun shot and shrapnel wounds, as well as the typical sprains, strains, broken bones, etc. that any athlete might suffer on a playing field. There were also the invisible wounds of post traumatic stress syndrome, bringing about nightmares, sleep disturbances, depression, and other psychological impairments.
yes she does suffer from asthma!!
There is a 100% probability of his child having Marfan's syndrome. The syndrome is carried by the FBN1 gene, and is dominant so there is no way to avoid having the disease. However the severity of it may vary from mild to severe, so his child may suffer from a mild form of the syndrome.
Sounds like epilepsy.
Patients with Marfan are more likely to develop pes planus (flat feet) or so-called "claw" or "hammer" toes than people in the general population. They are also more likely to suffer from chronic pain in their feet.
I think it is real. Lots of people suffer from this syndrome. I think it is real. Lots of people suffer from this syndrome. I think it is real. Lots of people suffer from this syndrome.
Yes they have hallow bones because some of them suffer from marfan
Antione B. MarfanMarfan syndrome was first described by a French doctor named Antione B. Marfan, who reported that one of his patients, Gabrielle, had especially long fingers (he called this arachnodactyly, or spider-fingers), skeletal abnormalities (including arms that were disproportionately long), and high, arched pallets. He also noticed spine defects. Antione noted that these traits seemed to be inherited, and it is now certain that Marfan syndrome is a hereditary disorder, and the gene for it is autosomal dominant A dominant gene is one that will overwrite other genes so that only one is required for the trait that that particular gene carries to be expressed. A person who inherits a dominant gene from one parent will automatically have the trait that the gene produces, unlike with recessive genes in which a gene for the trait must be inherited from each parent for the trait to show. Autosomal means that the gene is on a non-sex chromosome. There are 46 chromosomes in every human cell, and they make 23 pairs, each one connected by a centrome. The 23rd pair consists of the sex chromosomes.The gene for Marfan syndrome is located on chromosome fifteen. This gene causes the occurrence of too many microfibrillar fibers in the connective tissue, which results in a lack of flexibility in the body's tissues.Marfan syndrome almost always occurs as an inherited trait (about 75% of the time), but it can sometimes show up spontaneously in a person from a family that has never shown any signs of the disorder. Marfan syndrome, because it is dominant, will not skip generations (a recessive gene can be passed on without showing up for many generations, because two are needed for the trait to show, but if a dominant gene is going to show up, it will do so right away). Marfan syndrome has a 50% chance of being passed on to the children of an affected person. If the gene for Marfan syndrome is passed on, it will invariably show up, but the degree to which it shows its symptoms varies considerably, even within a family.Skeletal abnormalities that have been noticed in Marfan patients are a long face, an unusually tall stature, a short upper body in comparison to the lower body (because they have a short ribcage), and overgrown ribs. The latter results in chest deformities such as Pectus Excavatum (funnel chest) or Pectus Carnatum (pigeon breast). A wide pelvis, elongated skull, and prominent shoulder blades are other symptomsOne of the most distinctive characteristics of Marfan's Syndrome is unusually long arms, fingers, and toes. These skeletal problems can show up in either childhood or adolescence, and sometimes they do not show up at all Extremely mobile joints are another common characteristic.A good many patients have eye problems, like dislocated lenses, severe nearsightedness, iridodensis (a quivering motion of the iris), cataracts, detaching retinas, and glaucoma.The life-threatening risk to Marfan syndrome is that the aorta can grow to be too large, develop weak spots (aneurysms) and then tear (dissect). Without surgery, a person can die.People with Marfan's Syndrome often suffer from various lung problems as well.For more information www.marfan.org
It depends. If you have the genes or your family is Tall, you might grow taller like them. I know that women's stop growing at the age of 18 and men at the age of 21:)
Yes
no
No.
There have been no reports of specific celebrities publicly disclosing that they suffer from Gardner syndrome. This is likely due to the private and sensitive nature of medical conditions.
no it doesn't jake you suffer from down syndrome