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Children with Marfan syndrome may require a comprehensive medical management plan that includes regular monitoring by a cardiologist to assess heart and aortic health, as cardiovascular complications are common. They may also need orthopedic evaluations to address any skeletal issues, such as scoliosis. Additionally, vision assessments by an ophthalmologist are essential, as Marfan syndrome can lead to eye problems like lens dislocation. Early intervention and a multidisciplinary approach can help manage symptoms and prevent complications.
What else can I help you with?
What does Marfan syndrome mean?
Marfan Syndrome is a medical problem with the Conective Tissue.
What chromosome pair is affected by marfan syndrome?
17
What is the inheritance pattern to Marfan Syndrome?
Marfan syndrome is an autosomal dominant disorder. An affected person has a 50% chance of passing it on to each offspring, regardless of gender.
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 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.
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.
How common is Marfan syndrome in the general population?
How Common Is Marfan Syndrome?According to the National Marfan Foundation - Marfan.org - 1 in every 5,000-7,000 babies born is a child with Marfan syndrome. Other statistics about Marfan syndrome75% of people with Marfan syndrome have an affected parent.Approximately 25% of all cases are due to de novo(spontaneous) genetic mutations. This means they are the first person in their family to be affected.Marfan syndrome is an autosomal dominant mutation; this means that, if the mutation is present, the person has the syndrome to at least a mild degree. It can not skip generations. A person with Marfan has a 50% chance of passing it on to their children.Estimates indicate that approximately 0.02% of the global population has Marfan syndrome.Marfan syndrome is found equally in all ethnicities.
Is marfan syndrome automsomal dominant?
Yes, Marfan syndrome is autosomal dominant.
Is Marfan syndrome contagious?
Marfan's syndrome is not contagious. A person can only get it by inheriting it from a parent.
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 effects can marfan syndrome have on a persons life?
They cant exercise as vigorously as someone without Marfan syndrome
