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Symptom Checker » Fatigue » Gait disorder
 

Fatigue and Gait disorder
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Fatigue and Gait disorder

Fatigue:

Gait disorder:

Results: Causes of Fatigue AND Gait disorder

    1. Amyotrophic lateral sclerosis
     A motor neuron disease involving progressive degeneration and eventual destruction of the function of nerves that control voluntary movement....read more »
    2. Ankylosing spondylarthritis
     Inflammation of one or more spine joints. The spine becomes progressively painful and stiff and the spine joints may eventually fuse and cause disability. The condition may vary from mild to severe. Inflammation can affect other joints and tissues....read more »
    3. Discitis
     A subacute infection of the vertebral discs that usually occurs in children....read more »
    4. Felty Syndrome
     A rare complication of long-term rheumatoid arthritis which involves an enlarged spleen and blood abnormalities....read more »
    5. Hyperparathyroidism
     Increased secretion of parathyroid hormone from the parathyroid glands....read more »
    6. Multiple Sclerosis
     Autoimmune attack on spinal nerves causing diverse and varying neural problems....read more »
    7. Osteoarthritis
     Osteoarthritis is a chronic condition characterised by mechanical disrturbances due to degradation of joints. It is the most common form of arthritis, and the leading cause of chronic disability....read more »
    8. Paget's Disease
     Breast carcinoma involving nipple and areola....read more »
    9. Polio
     Dangerous virus now rare due to vaccination....read more »
    10. Sickle Cell Anemia
     Sickle cell anemia is an inherited blood disorder characterized by red blood cells which are crescent-shaped rather than the normal doughnut shape. These abnormally shaped red blood cells are unable to function normally and tend to undergo premature destr...read more »

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Results: 3184 causes of Fatigue OR Gait disorder

    1. 2-Hydroxyglutaricaciduria
     A rare metabolic disorder characterized by high levels of a certain chemical (2-Hydroxyglutaric) which causes a serious progressive neurological disease and damage to the brain. The features of this disorder are variable and some cases are milder than oth...more »
    2. 2-Methylbutyric Aciduria
     A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...more »
    3. 2-methylbutyryl-coenzyme A dehydrogenase deficiency
     A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...more »
    4. 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency
     A rare inherited disorder where lack of a certain enzyme (3-methylcrotonyl-Coa carboxylase) stops proteins with the amino acid leucine being metabolized normally by the body. The leucine builds up in the body and causes damage to the brain and nervous sys...more »
    5. 3 alpha methylcrotonyl-coa carboxylase 2 deficiency
     A rare inherited disorder where lack of a certain enzyme (3-methylcrotonyl-Coa carboxylase) stops proteins with the amino acid leucine being metabolized normally by the body. The leucine builds up in the body and causes damage to the brain and nervous sys...more »
    6. 3-alpha-Hydroxyacyl-CoA Dehydrogenase Deficiency
     A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activit...more »
    7. 3-alpha-hydroxyacyl-coenzyme A dehydrogenase deficiency
     A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activit...more »
    8. 3-methylcrotonyl-CoA carboxylase deficiency
     A rare inherited disorder where lack of a certain enzyme (3-methylcrotonyl-Coa carboxylase) stops proteins with the amino acid leucine being metabolized normally by the body. The leucine builds up in the body and causes damage to the brain and nervous sys...more »
    9. Abdominal Cancer
     Growth of abnormal cells (tumour) affecting the organs in the abdominal cavity; may be due to primary growth of a tumour or spread from another tumour (metastases, secondary tumour)...more »
    10. Abdominal abscess
     An abscess that occurs anywhere in the abdomen....more »

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Notes About Causes

  • Warning - Beta version - information may be incorrect (details)
  • Disclaimer - Do not use this information for diagnosis (details)
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