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Symptom Checker » Face blueness » Failure to thrive
 

Face blueness and Failure to thrive
Symptom Checker

Face blueness and Failure to thrive

Face blueness:

Failure to thrive:

Results: Causes of Face blueness AND Failure to thrive

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

Results: 810 causes of Face blueness OR Failure to thrive

    1. 14q+ syndrome
     A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....more »
    2. 18p minus syndrome
     A rare chromosomal disorder where a portion of chromosome 18 is missing which is characterized by mental and growth deficiencies, drooping upper eyelid and prominent ears. The type and severity of symptoms is determined by the amount of genetic material t...more »
    3. 1q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    4. 2q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    5. 3-Hydroxyisobutyric aciduria
     A rare inborn metabolic disorder which causes brain and facial anomalies, seizures and growth problems....more »
    6. 3-M Syndrome
     A rare genetic condition which is characterized by distinctive physical features and severe growth retardation that starts during the fetal stage. Intelligence is not affected....more »
    7. 3-methylglutaconic aciduria, type 4
     A rare genetic disorder where the body's cells are unable to make sufficient energy resulting in an accumulation in the body of 3-methylglutaconic acid. Type 4 is characterized by symptoms which overlap type 1 and 3....more »
    8. 3q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 3 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    9. 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency
     A very rare metabolic disorder where a deficiency of a particular enzyme results in the urinary excretion of a chemical called hawkinsin. Symptoms start once the infant is weaned off breast milk....more »
    10. 49,XXXXX syndrome
     A rare chromosomal disorder that affects only females and involves body cells having five copies of the X chromosome instead of the normal two....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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