Doctor insights on:
What Is The Average Life Span Of Someone Who Has Eds Or Marfans
Generally, normal: People with eds generally have a normal lifespan. Though, those with the rare vascular type of eds have a high risk of sudden death from organ or vessel rupture. Heart-related complications can shorten the lifespan of people with marfan syndrome, though many live into their 60's and 70's (i.e. Normal lifespan) with careful medical management. ...Read more
Ehlers-Danlos Syndrome is a medical condition characterized by hypermobile joints, very elastic or stretchy skin that bruises easily, and other abnormalities. It is caused by defects in collagen, an important structural protein that is responsible for the strength of many different types of tissue including skin, ...Read more
Not rare at all: Flexibility of the joints, both large and small, is common. Many normal folks have this, and so do folks with certain genetic conditions, like eds and marfan syndrome, two of hundreds of genetic conditions that feature joint hyperextensibility. Are you worried about these conditions? Bring your concerns up with your regular doctor at your next check up. ...Read more
Stature and heart: Marfans people are tall, skinny, with valve problems, joint instability, but also have aortic problems. Ehlers danlos has hypermobility, subluxations, but also certain types of eds have tissue fragility, spontaneous pneumothorax, joint subluxation, and has difficulty healing. ...Read more
Yes: Marfan's syndrome patients die from complications of aortic valve widening. If this is treated with inderal, progression is slower and patients live longer. In addition, if heart valve surgey is performed electivelly patients live longer. Untrated patients have a life span of 32 years. ...Read moreSee 1 more doctor answer
Is it possible for someone to have a combo of connective tissue disorders such as Marfan syndrome and ehlers danlos syndrome?
Yes, but unlikely: Both Marfan syndrome (see http://www.nhlbi.nih.gov/health/health-topics/topics/mar/) and Ehlers Danlos syndrome (see http://www.nlm.nih.gov/medlineplus/ency/article/001468.htm) are conditions where mutations in proteins that are main components of connective tissue are abnormal which can result in a number of tissue abnormalities and possible health problems.Not likely both conditions at same time ...Read more
No: They are different but both share the same increased extensibility of joints. ...Read more
Is it possible to have extra stretchy skin without having some serious underlying condition like Ehlers-Danlos syndrome or Marfan Syndrome?
Several treatments!: Yes! children and adults with marfan syndrome can have gradual widening of the aorta - the major artery connected to your heart. Sometimes the aorta becomes so weak that it breaks. But your cardiologist can use an ultrasound machine to watch your aorta very carefully. She can treat you with medicines to slow down the enlargement, and your chest surgeon can even replace your aorta if necessary. ...Read moreSee 1 more doctor answer
An echocardiogram: If you have marfan syndrome, you should be aware that your cardiologist can use ultrasound to watch for the gradual enlargement of your aorta. Depending on your age, height, and weight, she can determine whether your aorta is growing larger than normal and recommend either medicine, like a beta blocker, or surgery to prevent dissection or rupture of the aorta. ...Read moreSee 1 more doctor answer
Rarely: Occasionally, a person with marfan syndrome will have normal height, but the majority of people with marfan syndrome tall. Even if people with marfan syndrome who have normal height, there long bones tend to be longer than typical, resulting in longer than typical arms, legs, and fingers. ...Read moreSee 1 more doctor answer
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