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Hypermobility Syndromes
Hypermobility Syndromes
by Alike Medical Team ∙ Updated on June 13, 2023
Additional names
This group contains additional names: - Hypermobility syndrome (loose joints) - Hyperflexibility - Hypermobility Syndrome - Benign Hyperflexibility
General
Hypermobility syndrome is a condition in which the joints are easily moved beyond the normal range that is expected from each specific joint. It is a benign condition, and is very common in children. It can also be an inherited trait, such as in Ehlers-Danlos syndrome (EDS) which is a group of relatively rare genetic disorders of connective tissue. Also, in Down syndrome and Marfan syndrome it is more common. There is a familial component to hypermobility syndrome, as some genes that are responsible for the production of collagen are familial. Symptoms usually get better in adulthood.
1,738 people with Hypermobility Syndromes are on Alike.
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Signs & symptoms
Symptoms of hypermobility syndrome may include susceptibility to injuries, joint pain, tendency to joint dislocation and sprains, scoliosis, and back pain.
Diagnosis
Hypermobility is diagnosed by physical examination by examination of the joints range of motion.
Treatment
Usually, there is no need to treat hypermobility syndromes, as it does not cause any symptoms. Joint pain can be relieved by pain medications, physical therapy could be advised.
Note
☝ We provide information on prescription and over-the-counter medicines, diagnosis, procedures and lab tests. This material is provided for educational purposes only and is not medical advice, diagnosis or treatment.
National Institutes of Health ∙ World Health Organization ∙ MedlinePluse ∙ Centers for Disease Control and Prevention
☝ All information has been reviewed by certified physicians from Alike
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Most PCPs will not diagnose this, unfortunately. You will probably need to go to a specialist. Doesn’t hurt to bring it up, but I don’t expect my PCPs to completely understand or even know how to manage EDS or **hypermobility**. My PCP mostly handles my POTS diagnosis although I’ve also been diagnosed with EDS. It’s unfortunate not many doctors know how to treat it or will even diagnose it, there’s a whole medical stigma against EDS especially hEDs .. I would encourage you to look into it a bit more especially talking to people who have it now. It takes people 4-5 + years to get diagnosed with hEDS after having issues simply because the lack of doctors with medical knowledge of the condition.
I don't have the first two things you mentioned, however I have the dental crowding. I also have smooth and fragile skin that is prone to scraping and scarring but it's not stretchy or too bruised compared to how clumsy I am. Would that be considered HSD instead of heds? I am just curious as I am just starting the process of getting help for **hypermobility**.
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