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Symptom Checker » Yellow stained teeth in children » Dystonia in children

Yellow stained teeth in children and Dystonia in children
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Yellow stained teeth in children and Dystonia in children

Yellow stained teeth in children:

Dystonia in children:

Results: Causes of Yellow stained teeth in children AND Dystonia in children

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

Results: Causes of Yellow stained teeth in children OR Dystonia in children

    1. Acidemia, methylmalonic
     An inborn error of metabolism where amino acids in the body aren't metabolized properly resulting in high levels of the acid throughout the body....more »
    2. Aromatic amino acid decarboxylase deficiency
     A rare inborn error of metabolism involving the deficiency of an enzyme (aromatic L-amino acid decarboxylase) needed to process aromatic amino acids. This results in a deficiency of neurotransmitters such as dopamine and serotonin. The condition manifests...more »
    3. Carbon Monoxide -- Teratogenic Agent
     There is strong evidence to indicate that exposure to Carbon Monoxide 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...more »
    4. Cerebral Palsy
     Any brain disorder causing movement disability...more »
    5. Congenital malformations
     Physical body or organ malformations existing at birth...more »
    6. Dental caries
     A destructive process causing decalcification of the tooth enamel leading to cavitation of the tooth...more »
    7. Encephalitis
     Dangerous infection of the brain...more »
    8. Epidermolysis bullosa
     A group of rare inherited skin diseases characterized by fragile skin which forms blisters with even minor injuries. The blisters can be painful and can occur anywhere on the skin and even inside the digestive tract....more »
    9. Fahr's Syndrome
     A rare neurologic disorder where calcium is deposited in various parts of the brain resulting in progressive loss of motor and mental function....more »
    10. GM1 gangliosidosis
     A rare biochemical disorder involving a deficiency of an enzyme (beta-galactosidase A) which results in the accumulation of harmful chemicals (GM1 gangliosides) in the central nervous system and other body tissues. Type 1 is a severe infantile form of the...more »

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