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Symptoms » Arm stiffness » Glossary
 

Glossary for Arm stiffness

Medical terms related to Arm stiffness or mentioned in this section include:

  • Alexander Syndrome: Brain myelin disorder causing mental degeneration.
  • Arm conditions: Conditions that affect the arm
  • Arm pain: Pain or discomfort of one or both arms
  • Arm symptoms: Symptoms affecting the arm
  • Brain symptoms: Symptoms affecting the brain
  • Burns: Injury from burns and scalds.
  • Chikungunya: A rare viral disease usually transmitted by mosquitoes and characterized by fever, rash and severe arthritis.
  • Claw hand: Claw hand is a deformity of the hand that causes abnormally bent fingers and gives the hand the appearance of an animal's claw.
  • Head symptoms: Symptoms affecting the head or brain
  • Hereditary spastic paralysis, infantile onset ascending: A rare inherited progressive condition where the muscles of the arms, legs and face become increasingly weak and stiff due to damage to nerve cells that control muscle movement. The legs are affected first and then the arms and face - the symptoms ascend up the body. This condition involves mutations in the same gene and overlapping symptoms with juvenile primary lateral sclerosis but the difference is that primary lateral sclerosis only involves degeneration of the upper motor neurons whereas infantile-onset spastic paralysis is more severe and involves degeneration of upper and lower motor neurons.
  • 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
  • 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.
  • Movement symptoms: Changes to movement or motor abilities
  • Multiple Sclerosis: Autoimmune attack on spinal nerves causing diverse and varying neural problems.
  • Multiple Sclerosis, Susceptibility To, 1: Multiple sclerosis is a nerve or spinal cord disease that causes random damage to parts of the nervous system. The result is a diverse range of possible symptoms depending on which parts of the cord are damaged, and how often the inflammation reoccurs. Typical symptoms are any kind of tingling, numbness, burning sensations, "pins-and-needles" or other types of sensory changes in various parts of the body. Researchers have discovered that some forms of multiple sclerosis are linked to a genetic defect. Type 1 is linked to a defect on chromosome 6p21.3.
  • Multiple Sclerosis, Susceptibility To, 2: Multiple sclerosis is a nerve or spinal cord disease that causes random damage to parts of the nervous system. The result is a diverse range of possible symptoms depending on which parts of the cord are damaged, and how often the inflammation reoccurs. Typical symptoms are any kind of tingling, numbness, burning sensations, "pins-and-needles" or other types of sensory changes in various parts of the body. Researchers have discovered that some forms of multiple sclerosis are linked to a genetic defect. Type 2 is linked to a defect on chromosome 10p15.1.
  • Multiple Sclerosis, Susceptibility To, 3: Multiple sclerosis is a nerve or spinal cord disease that causes random damage to parts of the nervous system. The result is a diverse range of possible symptoms depending on which parts of the cord are damaged, and how often the inflammation reoccurs. Typical symptoms are any kind of tingling, numbness, burning sensations, "pins-and-needles" or other types of sensory changes in various parts of the body. Researchers have discovered that some forms of multiple sclerosis are linked to a genetic defect. Type 3 is linked to a defect on chromosome 5p13.2.
  • Multiple Sclerosis, Susceptibility To, 4: Multiple sclerosis is a nerve or spinal cord disease that causes random damage to parts of the nervous system. The result is a diverse range of possible symptoms depending on which parts of the cord are damaged, and how often the inflammation reoccurs. Typical symptoms are any kind of tingling, numbness, burning sensations, "pins-and-needles" or other types of sensory changes in various parts of the body. Researchers have discovered that some forms of multiple sclerosis are linked to a genetic defect. Type 4 is linked to a defect on chromosome 1p36.
  • 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
  • Osteoarthritis: A form of degenerative arthritis due to chronic degeneration
  • 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.
  • Raynaud's disease: It is a reversible ischemia of the peripheral arterioles. It is a painful sensation affecting the fingers and toes associated with whitening or redness
  • Raynaud's phenomenon: A condition where the body extremities sweat and turn blue and cold. Exposure to cold, emotional stress and smoking may trigger the condition. Also known as acrocyanosis.
  • Rheumatoid arthritis: An autoimmune inflammatory condition which primarily affects the joints
  • Scleroderma, systemic: A rare autoimmune connective tissue disease where the body attacks parts of the body and causes scarring and thickness of the tissue. In the systemic form, the skin and organs are involved.
  • Stiff arm: Reduced mobility or movement of the arm
  • Stiffness: Reduced mobility or movement
  • Syringomyelia: Spinal cord cysts
  • Tetanus: A disease caused by chemicals which are produced by a bacterium (clostridium tetani) and are toxic to the nerves. The infection usually occurs when the bacteria enter the body through a deep wound - these bacteria are anaerobic and hence don't need oxygen to survive.

Conditions listing medical symptoms: Arm stiffness:

The following list of conditions have 'Arm stiffness' 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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