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1.Skeletal system - grow above average height
2.cardiovascular system - undue fatigue shortness of breath etc
3. Eyes - nearsightedness
4.cns - weakening of the membrane that encases the spinal cord
5. Lungs - risk factor for pneumothorax (air escapes into the viseral pleura)
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What major organ systems are affected by Marfan syndrome?
Marfan syndrome affects three major organ systems of the body: the heart and circulatory system, the bones and muscles, and the eyes.
WHAT race does Marfan syndrome affect?
Marfan syndrome can affect people of any race or ethnicity. It is a genetic disorder that impacts the connective tissue in the body and is not specific to any particular race or population.
What is a Marfan Syndrome?
marfan syndrome is genetic disorder of connective tissue of the body. it cause a mutation of the gene that produces the protein fibrillin.
What is the Marfan Syndrone?
Marfan syndrome is a genetic disorder that affects the body's connective tissue, leading to a range of symptoms such as tall stature, long limbs, joint hypermobility, and heart defects. It can also affect the eyes, skeleton, and cardiovascular system. Treatment focuses on managing symptoms and preventing complications.
Is the disease marfan syndrome a chromosomal ad normality?
Yes. Marfan syndrome is caused by a defect (or mutation) in the gene that tells the body how to make fibrillin-1.
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.
What is an inherited syndrome marked by a tall thin body with arachnodactyly?
Marfan syndrome is an inherited disorder characterized by a tall, thin body with long limbs and fingers (arachnodactyly). Other features of Marfan syndrome include heart, eye, and skeletal abnormalities due to a genetic mutation affecting connective tissue. It can vary in severity and may require medical management to address associated complications.
What effect does Marfan syndrome have on the body?
It affects the body's production of fibrillin, which is a protein that is an important part of connective tissue.
Is gene therapy a possiblilty for marfan's syndrome?
Gene therapy is being explored as a potential treatment for Marfan syndrome, as it has the potential to correct the underlying genetic mutation that causes the condition. However, further research is needed to determine its safety and efficacy before it can become a standard treatment option for Marfan syndrome.
Is marfan syndrome pyshical or mental?
Marfan syndrome primarily affects the physical aspect of a person's health. It is a genetic disorder that primarily affects the connective tissue in the body, leading to physical symptoms such as long limbs, joint hypermobility, and heart problems. There is no evidence to suggest that Marfan syndrome directly affects mental health.
What year was Marfran syndrome discovered?
Named after Antoine Marfan, the French doctor who discovered it in 1896, Marfan syndrome is a disorder that affects the body's connective tissue, which is found everywhere in the body. Think of it as a type of "glue" that helps support all of your organs, blood vessels, bones, joints, and muscles.
Is marfan syndrome a genetic disease?
Yes, Marfan syndrome is a genetic disorder caused by a mutation in the FBN1 gene, which provides instructions for making a protein called fibrillin-1. This mutation affects the body's connective tissue, leading to various features and complications of the syndrome. It is inherited in an autosomal dominant pattern.
