There are several ways of getting diplegia in the arms.

There is no set course of progression for people with diplegia.

"For the majority of children with diplegia, growth and development are not a problem.

This should become apparent by the six month mark which means he or she does not have severe diplegia.

The treatment for facial diplegia depends on the underlying cause.

"This is the age range at which the child with diplegia makes the most significant physical improvement in motor function."

The term diplegia can refer to any bodily area, such as the face, arms, or legs.

Moderate diplegia means the person can usually walk but with a slight bend in the knees.

The most serious side effect of interferon is a spastic diplegia.

The most common infectious cause of facial diplegia is Lyme disease.

Parents suspecting diplegia should take their child to the doctor to potentially get an earlier diagnosis.

The most common symptom of a child with diplegia is stiff lower extremities.

No two people with spastic diplegia are exactly alike.

The intelligence of a person with spastic diplegia is unaffected by the condition.

People with severe diplegia usually need crutches, a walker, or a wheelchair to be able to get around.

Thus, for many years, spastic diplegia was known as Little's Disease; only later did the name change.

It is very common for people with Cerebral Palsy to have diplegia of the arms.

The most common cause of diplegia in the legs is Cerebral Palsy.

Spastic diplegia's social implications tend to vary with the intensity of the condition in the individual.

Thus diplegia usually refers to just symmetry of one body part or limb, as the legs, or arms.

Most people with spastic diplegia are fully ambulatory and have a scissors gait.

Children with diplegia are eventually able to walk, just normally later; they generally attend regular schools and become independently functioning adults."

Spastic diplegia (the lower extremities are affected with little to no upper-body spasticity).

Facial diplegia occurs in 50% of patients with Guillain-Barre Syndrome.

Many patients exhibit spastic diplegia, a condition characterized by increased muscle tone and spasticity in the lower body.