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Symptom Checker » Abnormal rigidity » Electrolyte imbalance
 

Abnormal rigidity and Electrolyte imbalance and Double Vision in Both Eyes and Fainting
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Abnormal rigidity and Electrolyte imbalance and Double Vision in Both Eyes and Fainting

  • Abnormal rigidity AND Electrolyte imbalance AND Double Vision in Both Eyes AND Fainting - Causes of All Symptoms
  • Abnormal rigidity OR Electrolyte imbalance OR Double Vision in Both Eyes OR Fainting - 2147 causes

Abnormal rigidity:

Electrolyte imbalance:

Double Vision in Both Eyes:

Fainting:

Results: Causes of Abnormal rigidity AND Electrolyte imbalance AND Double Vision in Both Eyes AND Fainting

Note: Do not use for diagnosis; see limitations of results.

Results: 2147 causes of Abnormal rigidity OR Electrolyte imbalance OR Double Vision in Both Eyes OR Fainting

    1. 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 »
    2. 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 »
    3. 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 »
    4. 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 »
    5. 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 »
    6. 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 »
    7. 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 »
    8. Abdominal Aneurysm
     Dilatation of a section of the abdominal aorta, usually due to a weakness in the wall of the artery...more »
    9. Abetalipoproteinemia
     A rare disorder involving abnormalities in fat metabolism. The resulting insufficiency of fats and vitamins affect the normal development and function of the body....more »
    10. Acanthocytosis
     A rare disorder where most of the red blood cells are abnormal with spiny projections due to lipid abnormalities. The blood abnormality is seen in conditions such as abetalipoproteinemia, severe liver disease and severe malnutrition. Symptoms and prognosi...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)
  • Important - See your doctor - Only a doctor can give an accurate diagnosis (details)
 

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