Ehlers-Danlos Syndrome
Hypermobile EDS is a genetic disorder with a range of symptoms, including hypermobility of joints, a tendency to dislocate joints frequently, and chronic musculoskeletal pain. Patients also have unusually soft and elastic skin, indented scars, and a tendency to bruise easily. They also tend to have heavy menstrual periods and are prone to nosebleeds.
The disorder is one of several subtypes of Ehlers-Danlos syndrome, a rare genetic connective tissue disorder. Hypermobile EDS is the most common subtype. The syndrome is diagnosed through family history and clinical criteria. In rare cases, genetic testing may be necessary to determine the cause.
Most forms of EDS are inherited in an autosomal dominant manner. This means a child has a 50% chance of inheriting the disorder. It is also possible to have more than one type of EDS within a family. In most cases, hypermobile EDS affects more women than men. Genetic testing can be helpful in determining the cause of EDS.
The treatment of hypermobile EDS focuses on preventing severe complications. The primary complications of EDS include problems with the skin, cardiovascular system, and musculoskeletal system. Because of the skin's thin, stretchable, and velvety texture, the skin of patients with EDS is susceptible to wound healing complications. In order to alleviate wound pain, physicians may apply deep or superficial stitches. In addition, patients with EDS should be monitored for symptoms of low bone density or arthritis.
Hypermobile EDS Treatment
The goal of hypermobile EDS treatment is to manage symptoms and improve the quality of life of patients with the disorder. This treatment is often multidisciplinary and includes a variety of therapies. Patients with EDS often benefit from holistic or alternative approaches to treatment that do not require invasive procedures or specialized clinical tests. While many of these treatments are not covered by insurance companies, many are effective and can improve the quality of life of people with EDS.
Hypermobile Ehlers-Danlos syndrome, or hyperextensibility, is an inherited condition that affects the connective tissues. People with this condition often experience joint hypermobility and pain. They are also prone to injury due to the hypermobility of their joints. Patients with hypermobility may exhibit signs and symptoms such as bruising, poor wound healing, and pain in the affected joints. Patients may also display autonomic dysfunction and cardiovascular or gastrointestinal problems.
Hypermobile EDS treatment depends on the cause of the disease and the severity of the symptoms. In the most severe cases, EDS can cause sudden and unexplained pain. If you or a family member suffers from EDS, you should seek medical attention as soon as possible. Some patients even choose to wear a MedicAlert bracelet as an additional measure to alert medical personnel to possible symptoms.
A family physician with experience treating hypermobile EDS will oversee treatment. Genetic testing can help determine whether the patient has a family history of the disorder. If so, your physician may suggest a course of treatment.
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