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
Marfan's syndrome is a genetic disorder caused by defects in a protein called fibrillin that, along with collagen, provides most of the structural support of our tissues. Individuals with Marfan's are often tall, lanky, have long arm spans, and are hyperflexible. The most serious complication of Marfan's is caused by defects in the wall of the aorta, the large blood vessel that leaves the heart and supplies the ...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
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
See below:: Ehlers–danlos syndrome (eds) is a group of inherited connective tissue disorders, caused by a defect in the synthesis of collagen (type i or iii). Marfan's syndrome is a genetic disorder of the connective tissue. People with marfan's tend to be unusually tall, with long limbs and long, thin fingers. It is caused by defects in a gene called fibrillin-1. ...Read more
Have pectus carinatum, skin hyperelasticity and hypermobile thumbs. Normal ECHO in 2014 and 2016. Can you have those traits without EDS/Marfan?
Possible yes but-: -U should be tested 4 Marfan's. There R various degrees,& grade I is what U describe. ...Read more
Yes: Marfan's syndrome patients die from complications of aortic valve widening. If this is treated with inderal, (propranolol) 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
No: They are different but both share the same increased extensibility of joints. ...Read more
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
Is it possible to have extra stretchy skin without having some serious underlying condition like Ehlers-Danlos syndrome or Marfan Syndrome?
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