What is Ehlers Danlos type 2?
What is Ehlers Danlos type 2?
A rare systemic disease characterized by generalized joint hypermobility with recurrent joint dislocations, redundant and hyperextensible skin with poor wound healing and abnormal scarring, easy bruising, and osteopenia/osteoporosis.
Is EDS Type 3 rare?
Video: Hypermobility EDS – an update Vascular Ehlers Danlos syndrome (vEDS) is a rare disorder, estimated to affect between 1 in 50,000 and 1 in 200,000 people.
What is the most severe type of EDS?
SPONDYLODYSPLASTIC EDS results in short stature, joint hypermobility, and intellectual disability. VASCULAR EDS is the most serious type due to the possibility of a shortened lifespan. Minor trauma can lead to extensive bruising and skin tears. Arterial rupture is the most common cause of sudden death.
What is the life expectancy of hypermobile EDS?
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.
What is Ehlers-Danlos type 4?
Ehlers-Danlos syndrome type IV, the vascular type of Ehlers-Danlos syndromes (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous vessels on the trunk and lower back, easy bruising, and severe arterial …
Does EDS make you skinny?
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.
What is Ehlers Danlos type 4?
Does EDS get worse with age?
Many of the problems associated with EDS are progressive, meaning that they get worse over time.
Can you have EDS and be stiff?
If a person has hEDS, it will likely affect them in different ways throughout their lifetime, and the person may be diagnosed with many other conditions known to occur in those with hEDS. For example, three disease phases were proposed in a 2010 study: a “hypermobility” phase, a “pain” phase, and a “stiffness” phase.
Does EDS worsen with age?
EDS prognosis by disease type 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.
Can you live a full life with EDS?
EDS cannot be ‘cured’ but many people learn over time how to control it and live full and active lives. The day-to-day management of most types of EDS is based around the right kind of exercise, physiotherapy and pacing. In addition you should seek referrals for any associated conditions you may have.
What is Ehlers-Danlos type 6?
The Ehlers-Danlos syndrome type VI (EDSVI) is an autosomal recessive connective tissue disease which is characterized by severe hypotonia at birth, progressive kyphoscoliosis, skin hyperelasticity and fragility, joint hypermobility and (sub-)luxations, microcornea, rupture of arteries and the eye globe, and osteopenia.
How do you test for EDS syndrome?
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. This will show the doctor if there are any abnormalities present.
What causes Ehlers Danlos syndrome?
Causes of Ehlers-Danlos syndrome. Ehlers-Danlos syndrome is caused due to the various genetic mutations which result in the disruption of collagen production. The genetic mutations are generally passed on from one generation to another.
Who diagnoses Ehlers Danlos syndrome?
The diagnosis of one of the Ehlers Danlos syndrome is based on the findings of a medical history and physical exam. The doctor will test skin stretchiness and joint flexibility. Imaging tests can look for other signs and complications of EDS. A doctor can confirm the diagnosis of EDS through genetic tests performed on a blood sample.
What is the treatment for EDS syndrome?
physical therapy (used to rehabilitate those with joint and muscle instability)
