Ehlers–Danlos syndromes

From WikiMD's Wellness Encyclopedia

(Redirected from Ehlers-Danlos Syndrome)

Ehlers–Danlos syndromes (EDS) are a group of genetic disorders that affect the connective tissues that support the skin, bones, blood vessels, and many other organs and tissues. Defects in these tissues can lead to a variety of medical problems, ranging from mildly loose joints to life-threatening complications.

Etymology[edit | edit source]

The name Ehlers–Danlos syndrome (EDS) is derived from two physicians, Edvard Ehlers and Henri-Alexandre Danlos, who first described this condition at the turn of the 20th century.

Types[edit | edit source]

There are several types of EDS, each with its own set of symptoms and complications. These include:

Symptoms[edit | edit source]

Common symptoms of EDS include:

  • Joint hypermobility
  • Stretchy skin
  • Fragile skin that bruises or tears easily
  • Slow and poor wound healing
  • Development of scars that split open with little bleeding

Diagnosis[edit | edit source]

Diagnosis of EDS is typically based on clinical evaluation and family history. Genetic testing can confirm the diagnosis in some cases.

Treatment[edit | edit source]

There is currently no cure for EDS. Treatment is focused on managing symptoms and preventing complications.

See also[edit | edit source]

References[edit | edit source]

Ehlers–Danlos syndromes Resources

Contributors: Prab R. Tumpati, MD