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chapter 14

Terms and Definition

TermDefinition
Congenital anomalies defects present at birth
acute acute condition is a health issue that is severe and sudden in onset
Chronic a health issue that is ongoing and persists over a long period
Episodic a health issue that occurs in episodes
progressive one that becomes more and more serious or severe over time
Cerebral palsy a group of permanent disorders affecting movement, posture, and motor function due to non-progressive brain damage during early development.
quadriplegia all four limbs are involved
paraplegia only the legs are involved
hemiplegia one side of the body is involved
Spasticity stiffness or tenseness of muscles and inaccurate voluntary movement
Choreoathetoid abrupt, involuntary movements and difficulty maintaining balance
atonic floppiness or lack of muscle tone
seizure an abnormal discharge of electrical energy occurs in certain brain cells
epilepsy a chronic neurological condition and has recurrent seizures
Executive function a set of cognitive processes essential for controlling and regulating behavior, often compared to the role of a conductor of an orchestra, a movie director, or an air-traffic controller.
Adaptive behavior the collection of skills that enable individuals to meet the demands of everyday life.
Spina bifida a congenital defect where the spinal column does not close completely during fetal development, leading to the spinal cord and nerves being exposed and potentially damaged.
Neural tube defect a malformation involving the spine, spinal cord, or brain
Catheterization inserting a tube into an organ to inject or withdraw fluids
Muscular dystrophy a group of genetic disorders that cause progressive weakening and wasting away of muscles over time.
Juvenile rheumatoid arthritis an autoimmune disorder occurring before 16 years of age in which the muscles and joints are affected; the cause and cure are unknown
Scoliosis a condition characterized by an abnormal lateral curvature of the spine
asthma an increasingly common lung disease characterized by episodic inflammation or obstruction of the air passages such that the person has difficulty in breathing
Cystic fibrosis the most common autosomal recessive disease that leads to death
Acquired immune deficiency syndrome a life-threatening condition caused by the human immunodeficiency virus
Phenylketonuria a metabolic genetic disorder where the body cannot convert the amino acid phenylalanine into tyrosine
Neurotoxins toxic substances that specifically target the nervous system, causing damage to the brain, spinal cord, or peripheral nerves
prosthesis an artificial replacement for a missing body part
orthosis a device that enhances the partial functioning of a part of a person’s body
Adaptive devices special tools designed to help individuals with physical disabilities perform daily activities more easily.
Individualized family service plan a legal document required by federal law for infants and toddlers with disabilities.
Created by: giselleusc
 

 



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