0
What other inherited disease can be confused with Marfan syndrome?
GaleEncyofMedicine
The symptoms of Marfan syndrome in some patients resemble the symptoms of homocystinuria, which is an inherited disorder marked by extremely high levels of homocystine in the patient's blood and urine.
Wiki User
∙ 13y ago
Add your answer:
Earn +20 pts
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.
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 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.
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 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'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
