Met a family in a hospital waiting room with a family member with this disorder. I know very little:[ 1] Marfan syndrome is more commonly noted among a small subgroup of a certain type of exceptionally tall individuals.[2] It can "run in the family" so if it's in your family AND you are also exceptionally tall then you probably want to get yourself checked over by a special doctor that has had extra training about how to screen for Marfan syndrome as well as having had special training which focused on the latest research & additional knowledge about the specific way Marfan's syndrone affects people's body functions if they have it; [3] it is prudent to ask your own family doctor about Marfans syndrome first additionally then asking them about their own personal experience treating or diagnosing patients with this specific syndrome. (Some doctors may not be familiar with Marfans or only vaguely aware of what it is but unable to really provide specialized evaluation or treatment for it.) Best wishes.
it affects all races and all ages -- While just about every human can be either a carrier or posses Marfan Syndrome itself, animals can be effected as well.
Yes, Marfan Syndrome can be detected before birth through prenatal genetic testing such as chorionic villus sampling or amniocentesis. These tests can detect whether the fetus has inherited the genetic mutation that causes Marfan Syndrome. It's important to consult with a genetic counselor or healthcare provider for further information and testing options.
The cost of treatments for Marfan Syndrome can vary depending on factors such as the specific treatments needed, healthcare providers, insurance coverage, and geographic location. Treatment may include medications, monitoring, surgeries, and ongoing specialist care. It's best to consult with a healthcare provider and insurance company for a personalized cost estimate.
Since the traits for hemophilia are carried on the X chromosome and not the Y, it is more probable for females to have a chromosome with the mutation. Since the mutation is considered recessive and males only have one X chromosome, they are more likely to portray the phenotype for hemophilia than their female counterparts.
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.
While there is no cure for Marfan Syndrome (because it is a genetic disorder), there are ranges of treatment options can decrease (and even sometimes prevent) complications.
While there is no cure for Marfan Syndrome (because it is a genetic disorder), there are ranges of treatment options can decrease (and even sometimes prevent) complications.
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.
Yes, Marfan syndrome is autosomal dominant.
Marfan Syndrome is a medical problem with the Conective Tissue.
Marfan's syndrome is not contagious. A person can only get it by inheriting it from a parent.
No. Down is caused by an extra chromosome while Marfan is due to a mutation in one or more genes.
Marfan Syndrome is also known as Marfan's disease and hereditary connective tissue disorder. In some contexts, it may be referred to as Marfan syndrome type I or simply as a connective tissue disorder. However, the most common and widely recognized name remains Marfan Syndrome.
They cant exercise as vigorously as someone without Marfan syndrome
flat feet an sinked chest are some symptomes of marfan syndrome
Marfan syndrome is not naturally found in animals. However, researchers have created mice with Marfan syndrome in laboratories for the purpose of testing medications on them before conducting human trials.
The etiology of marfan syndrome would be the mutations in the protein FBN1 in the gene chromosome 15.