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Is Marfan syndrome a dominate disorder?
Yes Marfan syndrome is a dominate disorder that affects the bodies connective tissue. it also causes problems in the heart, eyes and bones
Why do Marfan syndrome sufferers develop longer bones?
Marfan syndrome causes an increase in the length of the patient's bones, with decreased support from the ligaments that hold the bones together.
What are the chances of getting marfan syndrome?
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.
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.
How Was Marfan Syndrome Discovered?
Marfan syndrome was first described by Antoine Marfan, a French pediatrician, in 1896. He observed a unique set of physical features in a 5-year-old girl, which led him to identify the syndrome as a distinct medical condition. Over time, further research and advancements in genetics have helped to better understand the underlying causes and manifestations of Marfan syndrome.
Is marfan syndrome automsomal dominant?
Yes, Marfan syndrome is autosomal dominant.
What does Marfan syndrome mean?
Marfan Syndrome is a medical problem with the Conective Tissue.
Is Marfan syndrome contagious?
Marfan's syndrome is not contagious. A person can only get it by inheriting it from a parent.
What are causes of Marfan syndrome?
It is a genetic disorder and if one parent has it, there is a 50?50 chance that the child will have it.
Is Down Syndrome the same as Marfan Syndrome?
No. Down is caused by an extra chromosome while Marfan is due to a mutation in one or more genes.
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.
What type of mutation causes marfan syndrome?
Marfan syndrome is typically caused by mutations in the FBN1 gene, which provides instructions for making a protein called fibrillin-1. These mutations can result in the production of an abnormal fibrillin-1 protein, leading to the characteristic features of Marfan syndrome such as tall stature, long limbs, and cardiovascular issues.
