Does EDS affect intelligence?
Although children with EDS may need special protection they also need to play and have friends. Involve your children in activities they can safely enjoy. Ehlers-Danlos syndrome does not affect intelligence but medical problems may interfere with progress in school or the child’s social or psychological adjustment.
Does hypermobile EDS shorten life expectancy?
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.
Can Ehlers-Danlos affect your voice?
Producing and maintaining voice is a reported difficulty. The way posture, breathing and the voice box need to coordinate to achieve a voice can be affected. It is becoming known that those with EDS can have respiratory difficulties, including asthma.
Does EDS worse 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.
Does Ehlers Danlos affect anesthesia?
Conclusions: No guidelines for neuraxial or general anesthesia exist for patients with Ehlers-Danlos syndrome, hypermobility type. Increased rates of cervical spine instability and local anesthetic resistance have been reported in this population and should be considered when developing the anesthetic plan.
Does Ehlers Danlos affect your 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.
How is a diagnosis of Ehlers Danlos made?
A diagnosis of the Ehlers-Danlos syndromes (EDS) is typically based on the presence of characteristic signs and symptoms. Depending on the subtype suspected, some of the following tests may be ordered to support the diagnosis: [1] [2] [3]
What’s the life expectancy of a person with Ehlers Danlos?
The long-term outlook ( prognosis) for people with Ehlers-Danlos syndromes (EDS) varies by subtype. 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.
Is there a cure for Ehlers Danlos syndrome?
Depending on the subtype, EDS may be inherited in an autosomal dominant or an autosomal recessive manner. There is no specific cure for EDS. The treatment and management is focused on preventing serious complications and relieving associated signs and symptoms.