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Symptoms » Intention tremor » Glossary
 

Glossary for Intention tremor

Medical terms related to Intention tremor or mentioned in this section include:

  • Alcohol abuse: Excessive alcohol as a symptom of other conditions
  • Alcohol intoxication: excess intake of alcohol can lead to serious consequences
  • Ataxia: Failure of muscular coordination
  • Ataxia -- hypogonadism -- choroidal dystrophy: A very rare disorder characterized by spinocerebellar ataxia, eye abnormalities and a failure of the pituitary to stimulate gonadal development during puberty.
  • Ataxia -- oculomotor apraxia, type 1: A nerve disorder which affects the motor nerves and results in movement problems which includes the eyes. Gait problems are usually the first symptom and this is followed by speaking difficulty, intention tremor and then eye movement problems.
  • Ataxia-oculomotor apraxia syndrome: A nerve disorder which affects the motor nerves and results in movement problems which includes the eyes. Gait problems are usually the first symptom and this is followed by speaking difficulty, intention tremor and then eye movement problems.
  • Autosomal Recessive Genetic Diseases: Any conditions that are related to any non-sex-determining chromosome
  • Brain symptoms: Symptoms affecting the brain
  • Cerebellar ataxia: Cerebellar ataxia is a form of ataxia originating in the cerebellum. Romberg's test can be used to distinguish cerebellar ataxia from other forms of ataxia
  • Cerebellar ataxia, X-linked: A disorder where degeneration of certain parts of the brain results in symptoms such as ataxia. The rate of progression can vary.
  • Cerebellar ataxia, autosomal recessive: A group of rare, recessively inherited neurological disorders caused by abnormalities in the cerebellum and spinal cord. In some cases other parts of the body may be affected.
  • Chemical poisoning -- Phosphine: Phosphine is a chemical used mainly in pesticides and rodenticides. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Communication symptoms: Symptoms related to problems with communication.
  • Coordination problems: Symptoms affecting physical coordination.
  • Dementia, familial Danish: A rare inherited form of dementia caused by the deposit of abnormal substances in the brain, spinal cord and retina and the degeneration of brain tissue. Deafness and cataracts usually started in the 20's with severe deafness occurring by the age of 45. Movement problems usually started after the age of 40 with death occurring in the 5th or 6th decade.
  • East Syndrome: A rare syndrome characterized mainly by mental retardation, deafness, ataxia and electrolyte imbalance.
  • Head symptoms: Symptoms affecting the head or brain
  • Hypomyelination -- congenital cataract: A rare syndrome characterized by the association of congenital cataract with progressive neurological impairment due to progressive demyelination.
  • Hypomyelination and congenital cataract: An inherited disorder characterized by congenital cataract and progressive neurological impairment due to reduced myelination of nerves.
  • Luteinizing hormone releasing hormone, deficiency of, with ataxia: A very rare syndrome characterized mainly by insufficient sex hormone production and impaired balance and coordination due to nervous system dysfunction.
  • Movement symptoms: Changes to movement or motor abilities
  • Multiple Sclerosis: Autoimmune attack on spinal nerves causing diverse and varying neural problems.
  • Muscle symptoms: Symptoms affecting the muscles of the body
  • Musculoskeletal symptoms: Symptoms affecting muscles or bones of the skeleton.
  • Myoclonus-ataxia: A rare syndrome characterized mainly by myoclonus and loss of movement coordination.
  • Nerve symptoms: Symptoms affecting the nerves
  • Neurological symptoms: Any symptoms that are caused by neurological conditions
  • Opsoclonus Myoclonus: Condition with involuntary muscle and eye movement.
  • Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa and Cataract: A very rare, recessively inherited condition characterized by the association of vision, hearing and neurological problems. The condition generally starts during the second decade of life and progresses slowly.
  • Robinson syndrome: A very rare condition observed in a West Coast Indian family. The condition is characterized by scoliosis, hearing impairment, ataxia and sensory loss. The severity, rate of progression and age of onset of the neuropathic symptoms was highly variable. Sensory symptoms tend to be most prominent in the hands and feet.
  • Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance: A rare syndrome characterized mainly by mental retardation, deafness, ataxia and electrolyte imbalance.
  • Speech symptoms: Problems with speech or voice.
  • Spinocerebellar ataxia 5: A genetic disorder involving progressive degeneration of the spinal cord resulting in symptoms such as incoordination and eye movement problems.
  • Spinocerebellar ataxia, autosomal recessive 2: A rare, recessively inherited brain disorder characterized by ataxia and mental retardation. The severity of the disorder is variable and the condition is nonprogressive.
  • Stroke: Brain-related symptoms of bleeding or blockage.
  • Stroke symptoms: Brain-related symptoms of bleeding or blockage.
  • Tremor: The occurrence of involuntary trembling
  • Tremor symptoms: Shaking or physical tremor.
  • Tumor: Abnormal tissue growth which may be malignant or benign.
  • Wilson's disease: Wilson disease, or hepatolenticular degeneration, is a neurodegenerative disease of copper metabolism.

Conditions listing medical symptoms: Intention tremor:

The following list of conditions have 'Intention tremor' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

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