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Spastic quadriplegia, also known as spastic tetraplegia, is a subset of spastic cerebral palsy that affects all four limbs (both arms and legs). Compared to quadriplegia , spastic tetraplegia is defined by spasticity of the limbs as opposed to strict paralysis .
Spastic CP is the most common type of overall cerebral palsy, representing roughly 80% of cases. [2] Spastic CP is a permanent condition and will affect an individual across the lifespan. [5] The brain injury that causes spastic CP remains stable over time, but the way spasticity affects a person can change. [1]
Spastic cerebral palsy affects the motor cortex [110] of the brain, a specific portion of the cerebral cortex responsible for the planning and completion of voluntary movement. [111] Spastic CP is the most common type of overall cerebral palsy, representing about 80% of cases. [112] Botulinum toxin is effective in decreasing spasticity. [10]
Tetraplegia, also known as quadriplegia, is defined as the dysfunction or loss of motor and/or sensory function in the cervical area of the spinal cord. [1] A loss of motor function can present as either weakness or paralysis leading to partial or total loss of function in the arms, legs, trunk, and pelvis.
The Gross Motor Function Classification System is a good indicator of hip issues, [88] [75] and more commonly occurs in children with spastic tetraplegia or spastic quadriplegia, but it is difficult to tell what type of CP a child has at the age where hip displacement might first become an issue (sometimes at 2 years old, but more commonly ...
I lost my autonomy and the life that I dreamed for myself." Like Owen, more than 300,000 people live with spinal cord injuries in the United States, with an estimated 18,000 new cases each year ...
The intelligence of a person with spastic diplegia is unaffected by the condition. Spastic tetraplegia (all four limbs affected equally). People with spastic quadriplegia are the least likely to be able to walk, or if they can, to want to walk, because their muscles are too tight and it is too much effort to do so.
HSP is also known as hereditary spastic paraparesis, familial spastic paraplegia, French settlement disease, Strumpell disease, or Strumpell-Lorrain disease. The symptoms are a result of dysfunction of long axons in the spinal cord. The affected cells are the primary motor neurons; therefore, the disease is an upper motor neuron disease. [2]