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What else can I help you with?
Can you catch the Marfan Syndrome from somebody the way you can catch the flu?
No, Marfan Syndrome is an inherited disorder of connective tissue. It is not an infectious disease.
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.
Will your children get marfan syndrome if you have it?
Yes, because this syndrome is inherited.
What are some symptoms of marfan syndrome?
people with marfan syndrome are typically very tall with loose jointed. people with marfan disease usually have long narrow faces.
What are other names for Marfan Syndrome?
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.
When did Antoine B. Marfan discover this disease?
Antoine Marfan, a pediatrician, discovered this disease in 1896. It is now called Marfan syndrome. It is a hereditary disorder of the connective tissue.
Dose marfan syndrome have to be on a x chormose?
Marfan syndrome is caused by a mutation in the FBN1 gene, which is located on chromosome 15 and is inherited in an autosomal dominant pattern. It is not linked to the X chromosome. Both males and females can inherit and display symptoms of Marfan syndrome.
Marfan syndrome who first clinically named this disease?
French doctor Bernard J.A. Marfan in 1896.
When marfan syndrome was discovered?
Marfan syndrome was first described by Antoine Marfan, a French pediatrician, in 1896. He identified the unique characteristics of the syndrome, including tall stature, long limbs, and heart problems.
Is marfan syndrome a genetic disease?
Yes, Marfan syndrome is a genetic disorder. It is not a disease. It is caused by a mutation in fibrillin and is an autosomal dominant mutation. This means that if you have a Marfan causing mutation, you have Marfan, and you have a 50/50 chance of passing it on to any children you may have. Severity of Marfan can vary within a family, even though all affected family members have the same mutation. It can not skip generations.
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.
Is Marfan's symdrome a transmitted disease?
Marfan's syndrome is a genetic disorder, so one would inherit it from their biological parents. You can't "catch" marfans syndrome
