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Symptoms » Hand tremor » Glossary
 

Glossary for Hand tremor

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

  • Alcohol Withdrawal: Symptoms that occur when alcohol consumption is discontinued or reduced. Symptoms may vary depending on the level of dependence.
  • Arm spasm: Involuntary contractions of muscles in the arm.
  • Arm symptoms: Symptoms affecting the arm
  • Autoimmune thyroid diseases: Autoimmune diseases of the thyroid gland.
  • Brain symptoms: Symptoms affecting the brain
  • Dystonia-Parkinsonism, Adult-Onset: A rare condition characterized by the association of parkinsonism and dystonia due to a neurodegenerative disorder which progresses quickly.
  • Emery-Nelson syndrome: A rare condition characterized by a flat face and hand and foot abnormalities.
  • Finger spasm: Sudden involuntary contraction of the muscles in the fingers .
  • Genetic Parkinson disease: A type of Parkinson disease that results from a genetic anomaly. There are a more than ten different genes that can cause Parkinson disease.
  • Hand conditions: Any condition that affects the hand
  • Hand pain: Pain affecting one or both hands
  • Hand symptoms: Symptoms affecting the hand
  • Hand tremor in children: Hand tremor in children is an involuntary trembling or shaking of a child's hand.
  • Hand tremors: The occurrence of a tremor that is evident in the hand
  • Head symptoms: Symptoms affecting the head or brain
  • Hyperthyroidism: The excessive activity of the thyroid gland
  • Idiopathic Parkinson's disease: Idiopathic Parkinson's disease is Parkinson's disease for which no particular cause can be determined - it is the most prevalent form of the condition. Parkinson's disease is a chronic, progressive, degenerative brain disorder characterized by tremors, muscle rigidity and slowed movements.
  • Leg symptoms: Symptoms affecting the leg
  • Limb symptoms: Symptoms affecting the limbs
  • Lithium poisoning: A type of heavy metal poisoning caused by excessive exposure to lithium.
  • Mitochondrial Parkinson's disease: A form of Parkinson's disease that seems to be linked to mitochondrial defects - mitochondria are the energy-producing components of body cells. Parkinson's disease is a chronic, progressive, degenerative brain disorder characterized by tremors, muscle rigidity and slowed movements.
  • Monomelic Amyotrophy: Rare motor neuron disease with good prognosis.
  • Movement symptoms: Changes to movement or motor abilities
  • Muscle spasm: The occurrence of a sudden prolonged and uncontrolled contraction of a muscle
  • Muscle symptoms: Symptoms affecting the muscles of the body
  • Musculoskeletal symptoms: Symptoms affecting muscles or bones of the skeleton.
  • Nerve symptoms: Symptoms affecting the nerves
  • Neurological symptoms: Any symptoms that are caused by neurological conditions
  • Neurosyphilis: Syphilis affecting the nervous system.
  • Olivopontocerebellar Atrophy: A group of diseases progressive degeneration occurs in a particular area of the brain (olivopontocerebellar area) which results in various neurological symptoms.
  • Parkinson disease 10 (PARK10): Type 10 Parkinson disease is linked to a genetic mutation on chromosome 1p32. Parkinson's disease is a chronic, progressive, degenerative brain disorder characterized by tremors, muscle rigidity and slowed movements.
  • Parkinson disease 11 (PARK11): Type 11 Parkinson disease is linked to a genetic mutation on chromosome 2q21.2. Parkinson's disease is a chronic, progressive, degenerative brain disorder characterized by tremors, muscle rigidity and slowed movements.
  • Parkinson disease 12 (PARK12): Type 12 Parkinson disease is linked to a genetic mutation on chromosome Xq21-q25. Parkinson's disease is a chronic, progressive, degenerative brain disorder characterized by tremors, muscle rigidity and slowed movements.
  • Parkinson disease 13 (PARK13): Type 13 Parkinson disease is linked to a genetic mutation on chromosome 2p12. This form of the condition tends to progress slowly. Parkinson's disease is a chronic, progressive, degenerative brain disorder characterized by tremors, muscle rigidity and slowed movements.
  • Parkinson disease 2, autosomal recessive juvenile (PARK2): Type 2 Parkinson disease is juvenile form of the condition and is linked to a genetic mutation on chromosome 6q25.2-q27. The condition may be inherited in a recessive manner and symptoms tend to be milder following sleep. Parkinson's disease is a chronic, progressive, degenerative brain disorder characterized by tremors, muscle rigidity and slowed movements.
  • Parkinson disease 3, autosomal dominant Lewy body (PARK3): Type 3 Parkinson disease is linked to a genetic mutation on chromosome 2p13. Parkinson's disease is a chronic, progressive, degenerative brain disorder characterized by tremors, muscle rigidity and slowed movements.
  • Parkinson disease 4, autosomal dominant Lewy body (PARK4): Type 4 Parkinson disease is linked to a genetic mutation on chromosome 4q21. This form of the condition tends to start around the age of 45 years and progresses rapidly. Parkinson's disease is a chronic, progressive, degenerative brain disorder characterized by tremors, muscle rigidity and slowed movements.
  • Parkinson disease 5 (PARK5): Type 5 Parkinson disease is linked to a genetic mutation on chromosome 4p14. Parkinson's disease is a chronic, progressive, degenerative brain disorder characterized by tremors, muscle rigidity and slowed movements.
  • Parkinson disease 6, autosomal recessive early-onset (PARK6): Type 6 Parkinson disease is an early-onset form of the condition and is linked to a genetic mutation on the PINK1 gene on chromosome 1p36. The condition may be inherited in a recessive manner and symptoms tend to fluctuate during the day. Parkinson's disease is a chronic, progressive, degenerative brain disorder characterized by tremors, muscle rigidity and slowed movements.
  • Parkinson disease 7, autosomal recessive early-onset (PARK7): Type 7 Parkinson disease is linked to a genetic mutation in the DJ1 gene on chromosome 1p36. This form of the condition tends to start before the age of 40 years and progresses slowly. Parkinson's disease is a chronic, progressive, degenerative brain disorder characterized by tremors, muscle rigidity and slowed movements.
  • Parkinson disease 8 (PARK8): Type 8 Parkinson disease is linked to a genetic mutation on chromosome 1p32. This form of the condition tends to progress slowly. Parkinson's disease is a chronic, progressive, degenerative brain disorder characterized by tremors, muscle rigidity and slowed movements.
  • Parkinson disease 9 (PARK9): Type 9 Parkinson disease is linked to a mutation in the ATP13A2 gene on chromosome 1p36. This condition progresses rapidly and usually starts during the second decade of life. Dementia, eye movement problems and wasting of the brain tissue occur in addition to the typical symptoms of Parkinson's disease. Parkinson's disease is a chronic, progressive, degenerative brain disorder characterized by tremors, muscle rigidity and slowed movements.
  • Parkinson disease, familial, type 1 (PARK1): Type 1 familial Parkinson disease is linked to a genetic mutation on chromosome 4q21. Parkinson's disease is a chronic, progressive, degenerative brain disorder characterized by tremors, muscle rigidity and slowed movements.
  • Parkinson disease, genetic types: A type of Parkinson disease that results from a genetic anomaly. There are a more than ten different genes that can cause Parkinson disease.
  • Parkinson's Disease: Degenerative brain condition characterised by tremor.
  • Primary Parkinsonism: A type of Parkinson disease that results from a genetic anomaly. There are a more than ten different genes that can cause Parkinson disease.
  • Promethazine -- Teratogenic Agent: There is evidence to indicate that exposure to Promethazine during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Proximal spinal muscular atrophy, Adult, autosomal recessive: A rare, progressive neuro-muscular disease that occurs in adults. Nerve cells in the spinal cord are impaired resulting in loss of voluntary muscle control in various parts of the body. The lack of use of the muscle results in atrophy or weakness. Progression and prognosis is difficult to determine as individuals are affected to varying degrees.
  • Proximal spinal muscular atrophy, type 3: A rare inherited disorder where motor neuron degeneration causes progressive muscle weakness and atrophy. The proximal muscles tend to be more affected than the distal ones and the legs tend to be more affected than the arms.
  • Proximal spinal muscular atrophy, type 4: A rare, progressive neuro-muscular disease that occurs in adults. Nerve cells in the spinal cord are impaired resulting in loss of voluntary muscle control in various parts of the body. The lack of use of the muscle results in atrophy or weakness. Progression and prognosis is difficult to determine as individuals are affected to varying degrees.
  • Proximal spinal muscular atrophy, type IV: A rare, progressive neuro-muscular disease that occurs in adults. Nerve cells in the spinal cord are impaired resulting in loss of voluntary muscle control in various parts of the body. The lack of use of the muscle results in atrophy or weakness. Progression and prognosis is difficult to determine as individuals are affected to varying degrees.
  • Resistance to thyroid stimulating hormone: A very rare disorder where the body is unable to respond to thyroid stimulating hormone even though it is present in sufficient quantities. The problem lies in defective thyroid stimulating hormone receptors.
  • Roussy-Levy hereditary areflexic dystasia: An inherited ataxia (incoordination) involving muscle wasting, kyphoscoliosis and absence of tendon reflexes.
  • Shaking hands: A condition which is characterized by shaking of the hands
  • Shaky hands: A condition which is characterized by shaking of the hands
  • Spinal Muscular Atrophy type III: Type of SMA, a genetic motor neuron disease affecting nerves and muscles.
  • Spinal muscular atrophy, Adult form: A rare, progressive neuro-muscular disease that occurs in adults. Nerve cells in the spinal cord are impaired resulting in loss of voluntary muscle control in various parts of the body. The lack of use of the muscle results in atrophy or weakness. Progression and prognosis is difficult to determine as individuals are affected to varying degrees.
  • Spinocerebellar ataxia 14: A rare genetic disorder (chromosome 19q13.4qter defect) characterized by gait ataxia, tremors and dysarthria (speech disorder). The condition progresses slowly.
  • Spinocerebellar ataxia 19: A rare genetic disorder (chromosome 1p21-q21 defect) characterized by mild cognitive impairment and myoclonus. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types.
  • Spinocerebellar ataxia 27: A rare genetic disorder (chromosome FGF14; 13q34 defect) characterized by tremors, dyskinesia and psychiatric episodes. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types.
  • Thyroid disease: Any medical condition which affects the thyroid
  • Tremor: The occurrence of involuntary trembling
  • Tremor symptoms: Shaking or physical tremor.
  • Xanax withdrawal: Symptoms that occur when Xanax use is discontinued or reduced. Xanax is a central nervous system depressant. Symptoms may vary depending on the level of dependence.

Conditions listing medical symptoms: Hand tremor:

The following list of conditions have 'Hand 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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