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Known as trisomy 21 Extra chromosome attached to 21st pair of chromosomes Risks include: Sibling or mother with Down syndrome Older maternal age at time of conception Inherited genetic disorder causing: Developmental delay Cognitive impairment Pattern of unusual physical features |
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Condition involving developmental delay A wide variety of symptoms relating to: Communication Social interaction Sensation of discomfort Ability to purposefully shift attention Ability to play |
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Conductive or sensorineural hearing loss Central auditory processing disorder (CAPD) Auditory neuropathy (auditory dyssynchrony) |
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Dysarthria Speech slurred, indistinct, slow, or nasal Common causes Damage to nerve pathways Delayed development from hearing problems Slow maturation of the nervous system |
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Difficulty in articulating words due to emotional stress or to paralysis, incoordination, or spasticity of the muscles used in speaking. |
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Speech pattern is broken, interrupted, or repetitious. Stuttering |
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a motor disorder caused by damage to the brain, in which someone has difficulty with the motor planning to produce speech |
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affects lower extremities |
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affects upper and lower extremities |
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a reaction of the autonomic (involuntary) nervous system to overstimulation. It is characterized by paroxysmal hypertension (the sudden onset of severe high blood pressure) associated with throbbing headaches, profuse sweating, nasal stuffiness, flushing of the skin above the level of the lesion, slow heart rate, anxiety, and sometimes by cognitive impairment.[2] usually in association with spinal cord injury (SCI) or disease (e.g. multiple sclerosis). |
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Caused by cartilage loss or abnormal bone growth |
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Rheumatoid arthritis (RA) |
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Systemic inflammatory disease Can be mild or full-blown and fatal Affected joints are susceptible to fractures and dislocations. |
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Nonprogressive neurologic disorder from brain injury that may occur during: Fetal development Labor and delivery First 2 years of life Produces altered skeletal muscle function or contractions Produces altered skeletal muscle function or contractions |
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Genetic disorder characterized by increased mucus productions |
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Severe, incurable degenerative disorder involving the nervous system Immune cells attack myelin sheath, preventing nerve transmission. Presentation includes problems related to: Muscle coordination Muscle tone Altered sensation Gait disturbances |
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Incurable genetic diseases causing slow, progressive degeneration of muscle fibers Obvious facial muscle changes Altered gait Delayed psychomotor developmental milestones Changes in posture |
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Duchenne muscular dystrophy (DMD) |
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Characterized by: Enlarged heart muscle Heart dysrhythmias Scoliosis of the spine Gait disturbances |
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Rare autoimmune disorder affecting neuromuscular transmission Ocular: localized to eyelids and extraocular muscles Generalized: affecting respiratory and skeletal muscles |
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Drooping eyelids Double vision Difficulty speaking, chewing, or swallowing Muscle weakness in the extremities |
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Birth defect caused by improper development of fetal neural tube Causes exposure of the spinal cord and meninges |
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May be accompanied by: Negative impact on bowel and urinary elimination Scoliosis Other orthopedic disorders |
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Poliomyelitis/Postpolio Syndrome |
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Viral infection with significant morbidity and mortality Aggressive vaccination campaigns have eradicated the virus in many countries. Humans are the only known host. |
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Poliomyelitis/Postpolio Syndrome |
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Survivors are at risk for: Worsening of muscle weakness Muscle atrophy Renewed risk of respiratory insufficiency/failure Difficulty swallowing, impaired speech Significant pain or fatigue |
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Chronic autoimmune disorder causing widespread tissue inflammation |
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Joint swelling and discomfort Pleuritic chest pain Fever Photosensitivity Swollen lymph nodes Mouth sores |
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