How is marfan syndrome accquired
https://my.clevelandclinic.org/health/diseases/17209-marfan-syndrome
Marfan syndrome is a genetic disorder that is inherited, which means it is acquired from one's parents. It is caused by a mutation in the FBN1 gene, responsible for producing a protein called fibrillin-1. This protein is essential for forming connective tissues that provide strength and flexibility to various organs and structures in the body.
To further understand how Marfan syndrome is acquired, you can follow these steps:
1. Start by researching and familiarizing yourself with the basics of genetics and inheritance patterns.
2. Learn about the FBN1 gene and its role in producing fibrillin-1.
3. Understand that Marfan syndrome follows an autosomal dominant inheritance pattern. This means that a person with a mutated FBN1 gene has a 50% chance of passing the syndrome to each of their children.
4. Often, but not always, an affected individual has a parent who also has Marfan syndrome.
5. If a person with Marfan syndrome wishes to have children, they have a 50% chance of passing the condition to each child they have.
6. Genetic tests can be performed to confirm the presence of the FBN1 gene mutation and diagnose Marfan syndrome.
Remember, it is always important to consult with a healthcare professional or a genetic counselor for accurate and tailored information about conditions like Marfan syndrome.