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Breathlessness in children and Coma and Shallow respiration and Weak urination and Urinary problems
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Breathlessness in children and Coma and Shallow respiration and Weak urination and Urinary problems

  • Breathlessness in children AND Coma AND Shallow respiration AND Weak urination AND Urinary problems - Causes of All Symptoms
  • Breathlessness in children OR Coma OR Shallow respiration OR Weak urination OR Urinary problems - 1682 causes

Breathlessness in children:

Coma:

Shallow respiration:

Weak urination:

Urinary problems:

Results: Causes of Breathlessness in children AND Coma AND Shallow respiration AND Weak urination AND Urinary problems

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

Results: 1682 causes of Breathlessness in children OR Coma OR Shallow respiration OR Weak urination OR Urinary problems

    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. Abuse dwarfism syndrome
     Retarded growth, intelligence and social behavior due to child abuse. The child abuse can take the form of mental or physical cruelty or neglect....more »
    9. 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 »
    10. Accelerated hypertension
     Accelerated hypertension is a condition characterized by a rapid increase in blood pressure. The condition is a medical emergency which can cause organ damage if not treated promptly....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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