Ataxia sentence example
Its most effective use, however, is as a nerve tonic in paralysis agitans, locomotor ataxia, impotence and nervous exhaustion.
In humans they are characterized by ataxia, dementia and behavioral changes.
The mice also showed symptoms of defective muscular coordination called ataxia, which has been linked to oxidative stress.
Dogs cats and rabbits suffered from effects including ataxia, hypotension and seizures.
Leslie Burke has cerebellar ataxia, a degenerative disease.Advertisement
Cerebellum - occupies most of the posterior cranial fossa; damage produces ataxia, slurring of speech.
Nine patients developed ataxia early in the course of the disease.
Her research project is focused on the molecular basis of inherited ataxia in people living in the North East of England.
A representative mouse model for the spinocerebellar ataxia has previously been generated under an approved project license.
Nature Neuroscience, April 2003 Mouse mimics movement disorder Scientists have produced the first mouse with episodic ataxia.Advertisement
There has been a rapid deterioration with progressive ataxia, confusion and agitation.
To manage autosomal recessive cerebellar ataxia (ARCA) patients in specialist clinics and collect blood samples and clinical data.
This case had fore and hind limb ataxia but normal cranial nerve function.
The title, AtaXia, comes from Greek and indicates a medical condition interfering with muscular coordination.
The first presenting symptom is generally ataxia, a medical term used to describe an unsteady gait.Advertisement
The potential for iron overload to cause hypertrophy is demonstrated in Friedrich's ataxia.
Overdose has resulted in symptoms including nystagmus, ataxia, impaired consciousness and coma.
Another problem to watch for is a condition called ataxia; this is the inability to properly coordinate voluntary muscle movements.
With the exception of one Collie that displayed temporary ataxia (trouble walking) after an administered dose, no other problems were detected.
Friedreich's ataxia (FA) is an inherited, progressive nervous system disorder causing loss of balance and coordination, speech problems, and heart disease.Advertisement
Friedreich's ataxia is the most common inherited ataxia, affecting one in 50,000 people in the United States.
Ataxia in the arms follows, usually within several years, leading to decreased hand-eye coordination.
Direct DNA testing is available, allowing FA to be more easily distinguished from other types of ataxia.
A child with Friedreich's ataxia is entitled to an Individual Education Plan (IEP) through the Individuals with Disabilities Education Act (IDEA).
Neurologic abnormalities resulting in poor coordination and an unsteady gait (ataxia).Advertisement
The decreased coordination of movements (ataxia) associated with A-T first becomes apparent when a child begins to walk, typically between 12 and 18 months of age.
They become apparent after the onset of the ataxia, often between two and eight years of age.
Establishing a diagnosis for ataxia telangiectasia is most difficult in very young children, primarily because the full-blown syndrome is not yet apparent.
As of 2004, there is no cure for ataxia telangiectasia, thus specific therapy is not available, and treatment is largely supportive.
Any family touched by ataxia telangiectasia is forever affected.
A-T support groups have been organized by all major A-T organizations, such as the Ataxia Telangiectasia Children's Project, the National Ataxia Foundation (NAF), and the Ataxia Telangiectasia Medical Research Foundation.
A lack of balance and coordination with unsteady movements (ataxia) may also be present.
An example is ataxia, characterized by a lack of coordination while performing voluntary movements.
When a child has primarily motor delays, conditions such as cerebral palsy, ataxia, spina bifida, spinal muscular atrophy (withering) and myopathy may be present.
The most common ataxia is Friedreich's ataxia; in the United States, it affects one in 50,000 people, both male and female.
Cerebellar disorders cause inability to control the force, fine positioning, and speed of movements (ataxia).
Ataxia is particularly visible when the patient is walking.
Diagnosis of gluten ataxia offers hope of an effective, drug-free therapy for patients who formerly had no recourse for treatment.
The first neurological symptom was generally ataxia, 26 including cerebellar, limb or gait ataxia.
Ataxia telangiectasia (A-T), also called Louis-Bar syndrome or cerebello-oculocutaneous telangiectasia, is a rare, inherited disease that attacks the neurological and immune systems of children.
Ataxia means poor coordination, and the telangiectasia are tiny, red spider blood vessels which develop in A-T patients, especially on the whites of the eyes and on the surface of the ears.
Variations that cause disease are called mutations and A-T results from a defective gene, the ATM gene (for ataxia telangiectasia, mutated), first identified in 1995.
Spasticity, muscle weakness, coordination, ataxia, and scoliosis are all significant impairments that affect the posture and mobility of children and adults with CP.
According to The University of Chicago's Jack Miller Center for Peripheral Neuropathy, celiac disease has also been shown to cause ataxia, a condition marked by jerky uncoordinated muscle movements.