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Fruity breath odor in children and Ketosis
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Fruity breath odor in children and Ketosis

Fruity breath odor in children:

Ketosis:

Results: Causes of Fruity breath odor in children AND Ketosis

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

Results: Causes of Fruity breath odor in children OR Ketosis

    1. Aspirin -- Teratogenic Agent
     There is strong evidence to indicate that exposure to Aspirin 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 expo...more »
    2. Diabetic Ketoacidosis
     Life-threatening complication of high blood sugars and diabetes....more »
    3. Ethanol -- Teratogenic Agent
     There is evidence to indicate that exposure to Ethanol 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 an...more »
    4. Glycogen storage disease type 6
     A rare, generally mild form of inherited glycogen storage disease where a deficiency of phosphorylase b kinase leads to hypoglycemia and accumulation of glycogen in the liver....more »
    5. Glycogen storage disease type 6A, due to phosphorylase kinase deficiency
     A rare, generally mild form of inherited glycogen storage disease where a deficiency of phosphorylase kinase leads to hypoglycemia and accumulation of glycogen in the liver. Phosphorylase kinase deficiency can cause glycogen storage disease type VIa and/o...more »
    6. Marasmus
     A form of malnutrition caused by a severe deficiency of both protein and calories...more »
    7. Organic acidemia
     High blood levels of organic acids which is caused by abnormal protein metabolism. Maple syrup urine disease and propionic academia are examples of organic acidemias. Deficiency of certain metabolic enzymes one of the main causes of organic academia....more »
    8. Phenylketonuria
     A metabolic disorder where there is a deficiency of the enzyme phenylalanine hydroxylase which leads to a harmful buildup of the phenylalanine in the body. Normally the phenylalanine is converted into tyrosine. The severity of the symptoms can range from ...more »
    9. Pyruvate carboxylase deficiency, Group C
     A rare inherited disorder characterized by a deficiency of pyruvate carboxylase which leads to accumulation of lactic acid and other compounds which can have a toxic effect on the nervous system and body organs. Type C is a mild form of the condition....more »
    10. Type 1 diabetes
     Severe insulin-treated diabetes typically occurring in young people....more »

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  • 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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