Hypermobile joints occur in some very rare medical conditions, but can also occur in otherwise healthy and normal children. Children generally tend to be more flexible than adults, but those with hypermobile joints are capable of flexing and extending beyond normally observed limits for that particular joint. The movement is accomplished without undue force and without discomfort. Children with hypermobile joints also frequently have flat feet.

• Ehlers-Danlos syndrome
• Down syndrome
• Marfan syndrome
• Morquio syndrome
• Cleidocranial dysostosis

There is no specific care for the hypermobility. In many cases, people with hypermobile joints are at an increased risk for joint dislocation and other problems, and extra care may be needed to protect the joints. Consult your health care provider for specific recommendations.

• The ability to move a joint suddenly changes or decreases
• A joint suddenly appears misshapen (different than usual for that person)
• There is a loss of ability to use an arm or leg, or there is pain with movement of a joint

Hypermobile joints often accompany other symptoms that, taken together, define a specific syndrome or condition. A diagnosis is based on a family history, medical history and thorough physical evaluation.

Medical history questions that help document hypermobile joints in detail may include:

• When was it first noticed?
• Is it getting worse or more noticeable?
• Are other symptoms are also present, such as swelling or redness around the joint?
• Is there any history of joint dislocation, difficulty walking, or difficulty using the arms?

The physical examination will include detailed examination of the muscles and skeleton. The joints may be moved to determine the direction and extent of mobility.

Diagnostic testing will vary depending on what condition is suspected.