What is hypermobility arthralgia?

Hypermobility joint syndrome (HJS) means your joints are “looser” than normal. It’s typically referred to as being double jointed. It is a common joint or muscle problem in children and young adults, and is one of many connective tissue disorders.

What is the life expectancy of someone with Ehlers-Danlos syndrome type 3?

Patients with the classical and hypermobility forms of Ehlers-Danlos syndrome have a normal life expectancy. About 80% of patients with vascular Ehlers-Danlos syndrome will experience a major health event by age 40 and the life expectancy is shortened, with an average age of death of 48 years.

Is hypermobility EDS degenerative?

Hypermobility type (hEDS) Frequent joint dislocation and degenerative joint disease are common and associated with a baseline chronic pain, which affects both physical and psychological wellbeing.

Is Ehler Danlos painful?

Ehlers-Danlos syndrome tends to result in chronic pain and discomfort, often in the joints, muscles, or nerves. It can also cause stomach problems and headaches. Medication can be a crucial part of a pain management strategy for many people with Ehlers-Danlos syndrome.

Does hypermobility affect teeth?

Ehlers-Danlos syndrome (EDS) can adversely impact upon the function of the mouth and in turn potentially lessen quality of life. While many people with EDS not have any notable oral problems specifically due to EDS, this connective tissue disorder can affect the teeth and gums as well as the temporomandibular joint.

Is hypermobility linked to autism?

There is also increasing evidence that ASD is more common in individuals with joint hypermobility-related disorders than expected by chance. A Swedish national registry study has recently shown that there is a positive association between EDS and ASD or ADHD, and similar results have been observed for HSD.

Does EDS shorten your life?

The vascular type is typically the most severe form of EDS and is often associated with a shortened lifespan. People affected by vascular EDS have a median life expectancy of 48 years and many will have a major event by age 40.

Does hypermobile EDS get worse with age?

The most common types of EDS (classical, classical-like, and hypermobile) do not greatly affect life expectancy. However, symptoms may become more severe as patients age and joints that have been dislocated multiple times become painful. Everyone’s bones become weaker with age.

Does EDS make you skinny?

What Is Ehlers-Danlos Syndrome? Ehlers-Danlos syndrome (EDS) is a disease that weakens the connective tissues of your body. These are things like tendons and ligaments that hold parts of your body together. EDS can make your joints loose and your skin thin and easily bruised.

Can you live a long life with EDS?

People affected by vascular EDS have a median life expectancy of 48 years and many will have a major event by age 40. The lifespan of people with the kyphoscoliosis form is also decreased, largely due to the vascular involvement and the potential for restrictive lung disease.

Does hypermobility syndrome get worse?

Joint hypermobility syndrome is when you have very flexible joints and it causes you pain (you may think of yourself as being double-jointed). It usually affects children and young people and often gets better as you get older.

What is EDS Type 3?

EDS Type 3 is an inherited disorder of collagen production. Collagenous tissue is found throughout your body. If you have EDS Type 3, some of that collagenous tissue is defective.

What is eds disease prognosis?

Prognosis of Ehlers-Danlos Syndrome (EDS) Life expectancy for patients with the vascular form of EDS is shortened due to risk of heart and lung complications. For other types of EDS life expectancy and quality of life is normal, though caution is advised with some activities.

What is hypermobile EDS?

Hypermobile Ehlers-Danlos syndrome is an inherited connective tissue disorder that is caused by defects in a protein called collagen. It is generally considered the least severe form of Ehlers-Danlos syndrome (EDS) although significant complications can occur.

What are eds Genes?

Ehlers–Danlos syndrome (EDS) is an inherited connective tissue disorder with different presentations that have been classified into several primary types. EDS is caused by a defect in the structure, production, or processing of collagen or proteins that interact with collagen, such as mutations in the COL5A or COL3A genes.

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