Could I have type 3 (hypermobility) ehlers danlos syndrome or hypermobility syndrome? My parents don't have eds.

Unlikely. Ehlers danlos is an inherited condition, so if it doesn't run in your family, it's very unlikely that you have it. If your joints are unusually flexible you may just be more limber than normal. But if you are worried about it, see your doctor and find out for sure.
See details. The difference is a matter of degree. Eds is most often a recessively inherited disorder so parents usually do not have the disease.

Related Questions

What can someone do for hypermobility syndrome / ehlers-danlos syndrome?

Strengthen. Strengthening opposing muscle groups helps stabilize joints. Avoid concussive sporting activities such as tennis, but leap to activities suck as cycycling, ei. Stationary, or road (mtb) bike. But stabilizing your joints with my recommendations, which involved weight or machines is best. (machines are safeest, because your joints are tracked in a specific motion.) hypermobility causes arthritis. Read more...

What is the difference between ehlers-danlos syndrome hypermobility type 3 and double jointedness?

EDS-3 is formal Dx. Eds-3 is a formal diagnosis whereas the term double jointedness is a term used to describe someone with hyperlax joints. Hyperlaxity is a normal variant and is only worrisome if it results in pain or joint instability whereby the term is changed to patholaxity (pathologic joint laxity). Read more...

What are the signs of Ehlers Danlos Syndrome Hypermobility Type in a young child?

This is type 1- -it includes global ligamentous laxity, shortness of stature, though symmetrical, meaning proportions R normal. Type 1 seem 2 B spared eye &cardiac problems. Read more...
Joints are very loos. The joints are hyper-extendible and you can bend the wrists backwards a lot. Read more...

Good Afternoon, First of all, I would like to ask you if you are familiar with Ehlers-Danlos Syndrome (hypermobility type)? I was diagnosed with hEDS in 2011 by Geneticist LaDonna Immken, M.D. here in Austin. Often I have questions and my PCP and other

Hypermobility. Ehlers-Danlos syndrome type III (EDS Type III, hypermobility type) typically presents with loose ligaments and flexible joints. This can cause joint pain after activity. The skin is not usually overly stretchy. Type III are not subject to the usual complications of more serious types of EDS. A normal lifestyle is expected. Read more...