Instability of almost all joints can happen, but appear most often in the lower and upper extremities, with the wrist, fingers, shoulder, knee, hip, and ankle being most common. Family members, teachers, and friends should be informed about EDSs so they can accept and assist the child.
These tests help rule out other conditions that can easily be disguised as EDS, and help further specify what type of EDS a patient might have.
Talk to your doctor before trying any new kind of exercise. Treat your child like other children. Physicians may refer a patient to an orthotist for orthotic treatment bracing.
Here are some suggestions that may help you cope: Close monitoring of the cardiovascular system, physiotherapy, occupational therapy, and orthopedic instruments e. The condition can also affect tissue, organs, bones and blood vessels. Apart from joint hypermobility, skin manifestations provide an important clue and include soft, silky skin texture, semi-transparent dermis, and hyperelasticity.
This can be reached most easily when people take care to avoid injury and protect their health. Support groups can be immensely helpful for patients dealing with major lifestyle changes and poor health.
Patients commonly demonstrate easy bruising, scarring, and poor wound healing.
Identifying any significant health risks may help prevent severe complications by vigilant screening and lifestyle alterations.
Over-the-counter pain relievers — such as acetaminophen Tylenol, others ibuprofen Advil, Motrin IB, others and naproxen sodium Aleve — are the mainstay of treatment.
To decrease bruising and improve wound healing, some patients have responded to vitamin C. What to expect from your doctor Your doctor may ask some of the following questions: However, those with blood-vessel fragility have a high risk of fatal complications, including spontaneous arterial rupture, which is the most common cause of sudden death.
And when bathing or showering, mild soaps are more gentle on your body. It is inherited as an autosomal recessive genetic trait. A skin biopsy can be used to diagnose this disorder.
If vascular issues are present, an initial examination could also include an echocardiogram. Minimize stress on your hips, knees and ankles. Special recommendations for anesthesia in people with an EDS are prepared by orphananesthesia and deal with all aspects of anesthesia for people with an EDS.
EDS is not specifically listed as a covered disability by the U. The genetic connective tissue disorder, Loeys-Dietz syndromealso has symptoms that overlap with EDSs. People with EDSs also show a resistance to local anaesthetics.
Here are a few things you can do to safeguard yourself. However, physical appearance and features in several EDSs also have characteristics including short stature, large eyes, and the appearance of a small mouth and chin, due to a small palate.
In your initial examination you will assess your joint hypermobility using the Beighton Scalewhich results in a numerical value that will help define what type of EDS you may have.
Joint dislocations and scoliosis are common. Those planning to start a family should be aware of the type of EDS they have and its mode of inheritance how it is passed down to children.
Patients and surgeons report being dissatisfied with the results. Build a support system. Preparing for your appointment You might first bring your concerns to the attention of your family doctor, but he or she may refer you to a doctor who specializes in genetic diseases.
An Ehlers-Danlos syndrome diagnosis can be made when any of the three major criteria are present, these include skin hyper extensibility, poor wound healing and joint hypermobility. Is your skin extra stretchy? Your physical therapist might also recommend specific braces to help prevent joint dislocations.
Your doctor will want to know if any of your family members have ever been diagnosed with any type of EDS or have common symptoms.
Use assistive devices to minimize pressure on your joints. Because blood vessels are more fragile in some types of Ehlers-Danlos syndrome, your doctor may want to reduce the stress on the vessels by keeping your blood pressure low.
Walking, swimming, tai chi, recreational biking, using an elliptical machine or a stationary bike are all good choices. In an EDS, the skin can be pulled away from the body, but is elastic and returns to normal when let go.No cure is known for Ehlers–Danlos syndromes; treatment is supportive.
Close monitoring of the cardiovascular system, physiotherapy, occupational therapy, and orthopedic instruments (e.g., wheelchairs, bracing, casting) may be helpful. This can help with stabilizing the joints and preventing injury. Despite the relative lack of knowledge amongst today's medical professionals, Ehlers-Danlos Syndrome has a long history that dates as far back as Ancient Greece.
Ehlers-Danlos syndrome is a group of disorders that affect connective tissues supporting the skin, bones, blood vessels, and many other organs and tissues.
Defects in connective tissues cause the signs and symptoms of these conditions, which range from mildly loose joints to life-threatening. Many people with Ehlers-Danlos syndrome can benefit from seeing a psychologist or social worker.
Support groups, either online or in person, help people share common experiences and potential solutions to problems. Treatment. There is no specific cure for Ehlers-Danlos syndrome.
Individual problems and symptoms are evaluated and cared for appropriately. Physical therapy or evaluation by a doctor specializing in rehabilitation medicine is often needed.
Expectations (prognosis) People with EDS generally have a normal life span. Intelligence is normal.
The Ehlers-Danlos syndromes (EDS) are currently classified into thirteen subtypes. Each EDS subtype has a set of clinical criteria that help guide diagnosis; a patient’s physical signs and symptoms will be matched up to the major and minor criteria to identify the subtype that is the most complete fit.Download