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Yellow stained teeth in children and Choreoathetosis
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Results: Causes of Yellow stained teeth in children AND Choreoathetosis

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

Results: 74 causes of Yellow stained teeth in children OR Choreoathetosis

    1. 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency
     A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Sympt...more »
    2. Aceruloplasminemia
     A rare, recessively inherited neurodegenerative disorder characterized by a lack of ceruloplasmin in the blood. The lack of ceruloplasmin results in abnormal iron use in the body and leads to iron deposits in various body tissues such as the brain, pancre...more »
    3. 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 »
    4. Alopecia -- hypogonadism -- extrapyramidal disorder
     A rare syndrome characterized by alopecia, progressive movement problems and a lack of gonadal function which affects puberty....more »
    5. Alternating hemiplegia of childhood
     A rare neurological disorder involving paralysis on one side of the body that is only temporary but occurs often. The extent of the paralysis is variable....more »
    6. Amphetamine abuse
     Use of the stimulant drugs known as amphetamines or "speed"...more »
    7. Antiphospholipid syndrome
     An autoimmune disorder characterized by blood clots and pregnancy losses....more »
    8. Ataxia Telangiectasia
     A rare inherited childhood disorder involving progressive degeneration of the nervous system....more »
    9. Barakat syndrome
     A rare condition characterized by deafness, kidney disease and insufficiency parathyroid hormone production....more »
    10. Basal Ganglia Disease, Adult-Onset
     A rare disorder where a genetic mutation results in a neurological disease resulting from abnormal iron and ferritin deposits in the brain....more »
    11. Benedikt's syndrome
     Damage to a part of the brain (intremedullary part of midbrain) can result in various neurological symptoms which can vary depending on the exact location and extent of the damage. Limb and trunk symptoms tend to be on the opposite side the eye symptoms. ...more »
    12. Cerebral Palsy
     Any brain disorder causing movement disability...more »
    13. Ceroid lipofuscinosis, neuronal 4
     A rare inherited biochemical disorder involving the progressive accumulation of certain chemicals (lipopigments) in body tissues due to deficiency of an enzyme (palmitoyl-protein thioesterase 1) needed to process it....more »
    14. Chlorpromazine -- Teratogenic Agent
     There is evidence to indicate that exposure to Chlorpromazine (a neuroleptic drug) 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...more »
    15. Complicated migraine
     Complicated migraine includes chronic migraine, status migrainosus, persistent aura without infarction, migrainous infarction, and migraine-triggered seizure....more »
    16. Cornelia de Lange Syndrome
     A very rare disorder involving delayed physical development and various malformations involving the head, face and limbs. The severity of symptoms is variable....more »
    17. Dandy-Walker malformation with mental retardation, basal ganglia disease, and seizures
     A rare X-linked syndrome characterized mainly by mental retardation and seizures....more »
    18. De Barsy Syndrome
     A rare inherited disorder characterized by loose, inelastic skin, involuntary limb movements, cloudy corneas and other abnormalities....more »
    19. De Sanctis-Cacchione syndrome
     A rare genetic ectodermal disorder characterized by sunlight sensitivity, skin atrophy and pigmentation and skin tumors as well neurologic involvement....more »
    20. Dental caries
     A destructive process causing decalcification of the tooth enamel leading to cavitation of the tooth...more »
    21. Dentatorubral Pallidoluysian Atrophy
     A condition caused by an abnormality of the DNA sequence on chromosome 12...more »
    22. Encephalopathy due to GLUT1 deficiency
     A rare inherited metabolic disorder where a genetic mutation results in the deficiency of an enzyme called glutaryl-CoA dehydrogenase which is required to metabolise certain amino acids (lysine, hydroxylysine and tryptophan). Problems occur when these met...more »
    23. 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 »
    24. Ethotoin -- Teratogenic Agent
     There is evidence to indicate that exposure to Ethotoin (an anticonvulsant drug) 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 b...more »
    25. Francois dyscephalic syndrome
     A rare genetic disorder characterized by very small stature, microphthalmia, small pinched nose and hypotrichosis....more »
    26. Glutaric Acidemia Type I
     A condition which results in an inability to process the amino acids lysine, hydroxylysine and tryptophan...more »
    27. Glutaric aciduria 1
     A rare inherited metabolic disorder where a genetic mutation results in the deficiency of an enzyme called glutaryl-CoA dehydrogenase which is required to metabolise certain amino acids (lysine, hydroxylysine and tryptophan). Problems occur when these met...more »
    28. Glutaricaciduria type 1
     A rare inherited metabolic disorder where a genetic mutation results in the deficiency of an enzyme called glutaryl-CoA dehydrogenase which is required to metabolise certain amino acids (lysine, hydroxylysine and tryptophan). Problems occur when these met...more »
    29. Haas-Robinson syndrome
     A rare, recessively inherited disorder involving defective copper metabolism within the body which causes symptoms such as mental retardation, seizures and poor muscle tone....more »
    30. Henoch-Schonlein purpura
     A form of vasculitis (blood vessel inflammation) that affects blood capillaries and affects mostly the skin, kidneys, joints and stomach....more »
    31. Huntington's Disease
     Inherited disease causing progressive mental deterioration....more »
    32. Hydroxyacyl-coa dehydrogenase, type 2, deficiency
     A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Some ...more »
    33. Hyperglycemia
     High levels of glucose in the blood...more »
    34. Hypernatremia
     Increased blood sodium levels. Can be caused by excessive sodium levels but is more often a result of low water levels in the body....more »
    35. Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
     A very rare inherited metabolic disorder where ammonia builds up in the body due to a defect in the transport of ornithine which prevents ammonia being converted to urea and being excreted through the urine. The severity of the condition is variable....more »
    36. Hyperthyroidism -- Teratogenic Agent
     There is strong evidence to indicate that the development of hyperthyroidism 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 th...more »
    37. Hypoglycemia
     Low blood sugar level...more »
    38. Idiopathic basal ganglia calcification, childhood onset
     A rare disorder involving the buildup of calcium deposits in various parts of the brain. It manifests as degeneration of the nervous system....more »
    39. Infantile convulsions and paroxysmal choreoathetosis, familial
     A very rare inherited syndrome characterized mainly by convulsions during infancy and choreoathetosis which can occur randomly or be triggered by certain stimuli such as exercise....more »
    40. Injury
     Any damage inflicted in the body...more »
    41. Kernicterus
     A rare condition involving high blood levels of bilirubin which can also accumulate in the brain and lead to neurological problems....more »
    42. Kuf Disease
    43. Lesch-Nyhan syndrome
     Inherited biochemical disorder of purine metabolism caused by the virtual absence of an enzyme called hypoxanthine-guanine phosphoribosyltransferase or HPRT....more »
    44. Lupus
     Autoimmune disease with numerous effects on various organs and linings....more »
    45. Mental retardation, X-linked -- Dandy Walker malformation -- Basal ganglia disease -- Seizures
    46. Mental retardation, X-linked -- choreoathesis -- abnormal behavior
     A rare X-linked disorder characterized by mental retardation, abnormal behavior and a movement disorder. The disorder is inherited in a X-linked manner which means that only males display the full range of symptoms whereas female carriers may have mild or...more »
    47. Mitochondrial diseases
     Any of a group of mitochondrial disorders affecting cell metabolism and especially muscles....more »
    48. Neuroferritinopathy
     A rare disorder where a genetic mutation results in a neurological disease resulting from abnormal iron and ferritin deposits in the brain....more »
    49. Neuroferritinopathy (adult-onset basal ganglia disease)
     A rare disorder where a genetic mutation results in a neurological disease resulting from abnormal iron and ferritin deposits in the brain....more »
    50. Niemann-Pick disease
     A rare inherited biochemical disorder involving the deficiency of an enzyme (acid sphingomyelinase) needed to break down certain lipids which results in an accumulation of these lipids in the body....more »
    51. Nutritional deficiency
     Any deficiency of the nutrients that are required to sustain human life...more »
    52. Oculorenocerebellar syndrome
     A very rare syndrome characterized mainly by eye, kidney and brain abnormalities....more »
    53. Pantothenate kinase-associated neurodegeneration
     A rare, inherited, progressive neurological movement disorder where accumulation of iron in the brain causes degeneration of the nervous system....more »
    54. Paroxysmal kinesigenic choreoathetosis
     A rare inherited neurological disorder involving short, recurring attacks of involuntary movement. The attacks usually only last for 5 to 10 seconds....more »
    55. Phenytoin -- Teratogenic Agent
     There is evidence to indicate that exposure to Phenytoin 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 ...more »
    56. Polycythemia
     Excess red blood cells in the blood...more »
    57. Pregnancy
     The condition of supporting a fetus from conception till birth....more »
    58. Pyruvate decarboxylase deficiency
     A rare genetic disorder involving an enzyme (pyruvate decarboxylase) deficiency which results in symptoms such as failure to thrive, psychomotor retardation, small head, eye problems, increased blood ammonia levels and lactic acidosis which can result in ...more »
    59. Respiratory failure
     Failure of the respiratory system...more »
    60. Rheumatic fever
     An inflammatory disorder that can occur as a complication of untreated streptococcal bacterial infection such as strep throat or scarlet fever. The condition may affect the brain, skin, heart and joints....more »
    61. SCHAD deficiency
     A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Sympt...more »
    62. Schimke, X-linked, mental retardation syndrome
     A very rare syndrome characterized by mental retardation, abnormal involuntary movements and retarded growth....more »
    63. Spastic paraplegia 20, autosomal recessive
     A rare disorder characterized mainly by progressive stiffness, weakness and wasting of the lower leg muscles. The thumb muscle and speech is also affected....more »
    64. Spinocerebellar Ataxia
     A condition characterised by a failure of muscle coordination due to pathology arising in the spinocerebellar tract of the spinal cord...more »
    65. Striatonigral degeneration infantile
     A genetic neurological disorder caused by progressive damage to a part of the brain called the striatum....more »
    66. Sydenham chorea
     Brain disease causing involuntary movements or spasms....more »
    67. Tardive Dyskinesia
     The toxic neurological side effects of neuroleptic drugs that have been used long term....more »
    68. Tooth Abrasion
     The loss or erosion of the outer part of the tooth (enamel). Sometimes the inner structures of the tooth are also involved. The condition is often caused by brushing too hard but can also be caused by eating lots of acidic foods, acid reflux and excessive...more »
    69. Tourette Syndrome
     A neurological disorder involving vocal and movement tics where where uncontrollable movements or verbal utterances are made....more »
    70. Type 10 17b-hydroxysteroid dehydrogenase deficiency
     A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Sympt...more »
    71. Wilson's Disease
     Wilson disease, or hepatolenticular degeneration, is a neurodegenerative disease of copper metabolism....more »
    72. Xeroderma pigmentosum
     A rare pigmentary disease that is caused by an enzyme deficiency...more »
    73. Xeroderma pigmentosum, type 1
     A rare genetic disorder where the enzyme that repairs DNA damage done by UV radiation is defective. It is characterized by sensitivity to sunlight, skin pigmentation and atrophy and actinic skin tumors. The different types of xeroderma pigmentosum vary in...more »
    74. Xeroderma pigmentosum, type 2
     A rare genetic disorder where the enzyme that repairs DNA damage done by UV radiation is defective. It is characterized by sensitivity to sunlight, skin pigmentation and atrophy and actinic skin tumors. The different types of xeroderma pigmentosum vary in...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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