Marfan Syndrome Treatment Cost In India

Marfan syndrome is an inherited disorder that affects connective tissue, which is made up of fibers that support and anchor your organs and other body structures. The heart, eyes, blood vessels, and skeleton are the most commonly affected organs in Marfan syndrome. Marfan Syndrome Treatment in India usually includes medications to keep your blood pressure low to reduce the strain on your aorta. It is critical to monitor damage progression on a regular basis. Many people with Marfan syndrome eventually require aortic repair surgery. The Marfan Syndrome Treatment Cost in India is reasonable when compared to other developed nations. The success may be partly credited to the oncologist and the surgeons’ expertise and the cutting-edge medical technology utilized in the best Indian facilities. In addition to these benefits, India is quite popular due to its inexpensive costs without reducing clinical standards.

What Is Marfan Syndrome?

Marfan syndrome is a connective tissue disorder. Connective tissue holds your body together and supports many structures throughout your body. The connective tissue in Marfan syndrome is abnormal. As a result, your heart and blood vessels, bones, tendons, cartilage, eyes, skin, and lungs are all affected. Marfan syndrome patients are typically tall and thin, with unusually long arms, legs, fingers, and toes. Marfan syndrome can cause mild or severe damage. If your aorta — the large blood vessel that connects your heart to the rest of your body — is damaged, the condition can be fatal.

Marfan Syndrome Treatment Cost In India

Marfan Syndrome treatment Cost in India starts from INR 1,91,000 (2,300 USD). In comparison to other countries, the cost of Marfan Syndrome treatment in India is very low. Furthermore, the quality and standard of medical care and services are comparable to the best hospitals in the world. 

The cost of a medical package in India may vary depending on several factors such as the type of treatment, the technique used, the choice of hospital and city, the doctor’s experience, and many more. This is the primary reason why thousands of patients from all over the world choose to travel to India for medical treatment.

What Are the Symptoms of Marfan Syndrome?

Because the disorder can affect so many different areas of the body, the signs and symptoms of Marfan syndrome can vary greatly, even among members of the same family. Some people only have minor side effects, while others develop potentially fatal complications.

Symptoms of Marfan syndrome may include:

• Tall and slim build
• Extremely long arms, legs, and fingers
• A breastbone that protrudes or sinks inward.
• A high, arched palate, as well as crowded teeth
• Murmurs in the heart
• Nearsightedness to the extreme
• A spine that is unusually curved
• Feet that are flat

Because Marfan syndrome affects connective tissue, it can have a wide-ranging impact on your body, including your skeletal system, heart and blood vessels, eyes, skin, and organs:

• Physical Appearance
• Dental Issues
• Eye problems
• Heart and blood vessel problems
• Lung and skin changes

Consult your doctor or pediatrician if you suspect you or your child has Marfan syndrome. If your doctor suspects a problem, you will most likely be referred to a specialist for further assessment.

What Are the Causes of Marfan Syndrome?

Marfan syndrome is caused by a mutation in the gene that codes for the structure of fibrillin and elastic fibers, both of which are important components of connective tissue. This gene is known as fibrillin-1 (FBN1).

Marfan syndrome is usually inherited. The pattern is known as “autosomal dominant,” which means it affects both men and women equally and can be inherited from only one parent who has Marfan syndrome. Marfan syndrome patients have a 50% chance of passing the disorder on to their children.

A new gene defect occurs in 25% of cases due to an unknown cause. Marfan syndrome is also known as a “variable expression” genetic disorder because not everyone with Marfan syndrome has the same symptoms, and some people’s symptoms are worse than others.

Marfan syndrome manifests itself at birth. You may not be diagnosed until you are a teenager or young adult.

How Is Marfan Syndrome Diagnosed?

Because Marfan syndrome can affect tissue throughout your body, confirming the diagnosis and developing a treatment plan may require the involvement of a team of healthcare providers. First, they’ll take your medical history, perform a physical exam to look for typical Marfan syndrome signs or findings, ask you questions about your symptoms, and gather information about family members who may have had health problems related to Marfan syndrome.

The following tests may be used to evaluate changes in the heart, blood vessels, and heart rhythm problems or to directly diagnose Marfan’s syndrome:

• A chest X-ray is used to examine the border of your heart.
• An electrocardiogram (ECG) is used to check the rate and rhythm of the heart.
• Check for heart valve problems, ventricular dilation or thickening, aortic enlargement, dissections (tears), or aneurysms with an echocardiogram.

If your healthcare provider cannot see sections of the aorta on an echocardiogram or suspects a dissection has already occurred, you may require additional testing.

These includes:

• Transesophageal echocardiogram (TEE)
• MRI & CT Scan

A blood test can aid in the diagnosis of Marfan syndrome. This genetic test looks for changes in FBN1, the gene responsible for the majority of Marfan syndrome cases.

Because FBN1 test results are not always obvious, you should consult with a genetic counselor. Blood tests can also be used to help diagnose other genetic mutations that cause physical symptoms similar to Marfan syndrome, such as Loeys-Dietz syndrome.