Does Ehlers-Danlos affect mental health?

Does Ehlers-Danlos affect mental health?

What mental health problems are common in EDS? Research has shown that anxiety, depression, and other mood disorders are common in EDS patient populations. Somatoform disorders, where patients experience pain and fatigue without a known cause, are also common in patients with EDS.

How is Ehlers-Danlos hypermobility diagnosed?

There is no test for hEDS, so diagnosis involves looking for joint hypermobility, signs of faulty connective tissue throughout the body (e.g. skin features, hernias, prolapses), a family history of the condition, and musculoskeletal problems (e.g. long-term pain, dislocations).

Is Ehlers-Danlos a neurological disorder?

Ehlers–Danlos syndrome (EDS) is a heterogeneous heritable connective tissue disorder with various neurological manifestations, including chronic pain. The neurological manifestations in EDS are often regarded as being caused by the associated musculoskeletal disorders or polyneuropathy.

Can Ehlers-Danlos affect your brain?

Because EDS is a connective-tissue disorder, it is not commonly associated with the brain or the nervous system. However, there is evidence that some types of EDS can affect the brain. Studies have suggested that patients with EDS might be susceptible to damage to brain cells after even a mild traumatic head injury.

Do people with EDS have anxiety?

Many people with Ehlers-Danlos syndrome (EDS) deal with chronic pain and fatigue. This may contribute to the frequency of anxiety disorders among EDS patients. Indeed, some studies have indicated that anxiety affects more than half of those with hypermobile EDS.

Who diagnoses hypermobile EDS?

Most medical doctors should be able to diagnose EDS and HSD. However, because the Ehlers-Danlos syndromes are genetic disorders, primary care physicians often provide their patients with referrals to a geneticist.

What criteria is used to diagnose Ehlers-Danlos?

Extremely loose joints, fragile or stretchy skin, and a family history of Ehlers-Danlos syndrome are often enough to make a diagnosis. Genetic tests on a sample of your blood can confirm the diagnosis in rarer forms of Ehlers-Danlos syndrome and help rule out other problems.

Can neurologist diagnose Ehlers Danlos?

Although the global assessment of EDS patients is, by definition, multisystem and often managed by other specialists, such as rheumatologists and clinical geneticists, the neurologist has a high chance of evaluating still undetected EDS patients with a neurological presentation.

What tests are used to diagnose Ehlers Danlos Syndrome?

How is EDS diagnosed? Doctors may use a series of tests to diagnose EDS (except for hEDS), or rule out other similar conditions. These tests include genetic tests, skin biopsy, and echocardiogram. An echocardiogram uses sound waves to create moving images of the heart.

Can a neurologist diagnose Ehlers Danlos?

Are there any psychiatric disorders associated with Ehlers Danlos syndrome?

Ehlers-Danlos syndromes (EDS) are a heterogeneous group of hereditary connective tissue disorders characterized by joint hypermobility, widespread musculoskeletal pain and tissue fragility. Psychiatric disorders and psychosocial impairment are common, yet poorly characterized, findings in EDS patients.

What is the cause of hypermobile Ehlers Danlos syndrome?

Try our interactive tool for help finding information, services, experts, financial aid, and more! Hypermobile Ehlers-Danlos syndrome is an inherited connective tissue disorder that is caused by defects in a protein called collagen.

How are hypermobile EDS and hypermobility spectrum disorders diagnosed?

Hypermobile EDS and hypermobility spectrum disorders. Recently some changes were made to the way hypermobile Ehlers-Danlos syndrome is diagnosed. There is no test for hEDS, so diagnosis involves looking for joint hypermobility, signs of faulty connective tissue throughout the body (e.g. skin features, hernias, prolapses),…

Is there a difference between benign joint hypermobility syndrome and EDS?

The main differential diagnosis is other types of EDS, particularly those characterized by significant connective tissue abnormalities. There is still debate as to whether benign joint hypermobility syndrome (BJHS) is a distinct disorder or part of a clinical continuum.