What are 4 symptoms of Marfan syndrome?

Marfan syndrome features may include:

• Tall and slender build.
• Disproportionately long arms, legs and fingers.
• A breastbone that protrudes outward or dips inward.
• A high, arched palate and crowded teeth.
• Heart murmurs.
• Extreme nearsightedness.
• An abnormally curved spine.
• Flat feet.

Can Marfan be asymptomatic?

This condition usually does not cause symptoms (asymptomatic), but has been associated with lower back pain and can cause pinching of a nerve leading to abnormal sensations or muscle performance in the legs. Affected individuals may also developed stretch marks (striae atrophicae) of the skin without an obvious cause.

At what age is Marfan syndrome detected?

Their ages when the Marfan syndrome was first diagnosed ranged from 32 to 72 years (mean age, 46 years). Of these 28 patients, 7 were older than 50 years of age at the time of initial diagnosis.

Did you know facts about Marfan syndrome?

Marfan syndrome is a disorder that affects the body’s connective tissue. Connective tissue is the muscles, tendons, cartilage, and other parts that hold your bones, joints, organs, and tissues together. In Marfan syndrome, the connective tissue is weaker than normal so it stretches, bulges, or tears.

What is LOEY Dietz syndrome?

Loeys-Dietz syndrome is a connective tissue disorder that was first described in 2005. Most individuals with this disorder have craniofacial features that include hypertelorism (widely spaced eyes) and a bifid or broad uvula.

What is Noonan syndrome?

Noonan syndrome is a genetic disorder that prevents normal development in various parts of the body. A person can be affected by Noonan syndrome in a wide variety of ways. These include unusual facial characteristics, short stature, heart defects, other physical problems and possible developmental delays.

Can you have Marfan syndrome without being tall?

Not everyone who’s tall or thin or nearsighted has the disease. People who have Marfan syndrome have very specific symptoms that usually occur together, and it’s this pattern that doctors look for when diagnosing it.

Can a person with Marfan syndrome gain weight?

It could put too much pressure on my unstable joints, as well as increase the high blood pressure and cholesterol that I also have as a result of Marfan syndrome. Medical experts claim that most people with Marfan syndrome have difficulty gaining weight no matter how hard they try.

What is the life expectancy of someone with Marfan?

One in 10 patients may have a high risk of death with this syndrome due to heart problems. Despite the high risk for Marfan related cardiovascular problems, the average life expectancy of those with Marfan syndrome is nearly 70 years. The life expectancy in this syndrome has increased to greater than 25\% since 1972.

What are the signs of Marfan syndrome in children?

Experts recommend that pediatricians evaluate all children with sunken chest for other tell-tale Marfan signs, including long slender fingers, arm span exceeding height, long lean skull with downward slanted eyes and a spinal curvature (scoliosis), among others.

Is my body height 176 cm too high for Marfan syndrome?

Regarding thumb sign C, you should be able to do this sign easily, so you probably pushed it a little too had. A body height of 176 cm doesn’t sound like Marfan syndrome – unless when your length exceeds the body height of your family members significantly!

What are the symptoms of a sunken chest?

Symptoms of sunken chest Diagnosis can be clinical where the doctor just looks and sees the sunken chest. Other than the obvious defect, pectus excavatum can produce compressive symptoms because it presses on the heart and lungs. These symptoms include shortness of breath, chest pain, poor exercise tolerance, arrhythmias, and unusual fatigue.

Do you have stretch marks with Marfan syndrome?

In many cases, the patient has stretch marks on his or her body. A recent weight change can produce stretch marks in your skin. But stretch marks in Marfan Syndrome sufferers can be found even in the absence of a weight alteration. Picture 3: Stretch Marks (One of the symptoms of marfans syndrome)Source: emedicine.medscape