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Marfan syndrome is an inherited condition that affects the body's connective tissue, which provides structural integrity and support to many organs and structures. The condition primarily affects the heart, eyes, blood vessels, and skeleton, ranging from mild to severe damage. One of the most critical complications is the risk of aortal damage, which can be life-threatening if left untreated. Marfan syndrome is caused by a genetic mutation affecting the production of a specific protein essential for maintaining the elasticity and strength of connective tissue.
In Mysore, the best doctors for Marfan syndrome are available at Apollo Hospitals. These doctors for connective tissue disorder and doctors for aortic aneurysms are equipped with advanced tools and expertise to provide comprehensive care for patients with this condition.
Marfan syndrome does not have distinct stages or types, but the severity and manifestations of the condition can vary widely among individuals.
The symptoms of Marfan syndrome can vary significantly among individuals and even within families due to its broad impact on different areas of the body:
Physical features:
Long, narrow face
Tall and thin body build
Long arms, legs, fingers and toes
Breastbone that is protruding or indented
Eye problems:
Nearsightedness
Cataracts
Retinal detachment
Glaucoma
Heart problems:
Aortic aneurysm
Enlarged heart
Abnormal heart rhythm
Mitral valve prolapse
Lung issues:
Asthma
Recurrent bronchitis
Spontaneous pneumothorax (collapsed lung)
Skin changes:
Stretch marks due to less elastic skin
Easy bruising
Here are the steps used by the best doctors for Marfan syndrome at Apollo Hospitals in Mysore to diagnose this syndrome:
Family and Personal Medical History: Doctors inquire about family members with Marfan syndrome or early, unexplained heart-related conditions.
Physical Examination: The examination includes measuring arm and leg proportions, examining eyes, skin and musculoskeletal system, and listening to heart and lungs.
Imaging Tests: Tests may include CT scans, MRI, echocardiography and other imaging to evaluate heart, lungs and eyes.
Genetic Testing: Genetic testing is often used to confirm the presence of mutations in the FBN1 gene and to screen for associated genetic conditions.
Ghent Criteria: The diagnosis is confirmed by comparing the patient's signs and symptoms against the Ghent criteria, encompassing characteristic features associated with Marfan syndrome.
At Apollo Hospitals in Mysore, advanced facilities and highly experienced doctors for connective tissue disorders ensure each patient receives personalised care. The doctors specialising in Marfan syndrome treatment adopt a comprehensive patient-centric approach to manage this disorder, which may include:
Medications: Beta-blockers are prescribed to maintain lower blood pressure and reduce stress on the aorta, mitigating the risk of complications like aortic dissection.
Regular Monitoring: Tests such as echocardiograms and imaging scans are performed regularly to monitor the progression of aortic enlargement and other associated conditions.
Lifestyle Adjustments: Patients are recommended to avoid heavy lifting and competitive sports to reduce strain on the aorta.
Surgery: In some cases, preventive surgery may be required to repair an enlarged or torn aorta, lens removal for dislocated lenses or scoliosis surgery for severe spinal curvature.
Genetic Counselling: This involves educating patients and their families about the genetic aspects of Marfan syndrome, its inheritance patterns, and family planning considerations.
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