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Results 1 - 10 of 23 for Disorder of organic acid metabolism
  1. Newborn screening tests 
    ... Glucose-6-phosphate dehydrogenase deficiency (G6PD) Human immunodeficiency disease (HIV) Organic acid metabolism disorders Phenylketonuria (PKU) Sickle cell disease and other ...
    https://medlineplus.gov/ency/article/007257.htm - Medical Encyclopedia
  2. Newborn Screening Tests for Your Baby (March of Dimes Foundation)  
    Newborn Screening/Specifics ... Newborn Screening ... March of Dimes Foundation ... Newborn screening tests are essential for your baby. Understand their importance, ...
    https://www.marchofdimes.org/.../newborn-screening-tests-your-baby - External Health Links
  3. Phenylketonuria 
    ... Inborn errors of carbohydrate, ammonia, amino acid, and organic acid metabolism. In: Gleason CA, Sawyer T, eds. Avery's Diseases of the Newborn. 11th ed. Philadelphia, PA: Elsevier; ...
    https://medlineplus.gov/ency/article/001166.htm - Medical Encyclopedia
  4. Maple syrup urine disease 
    ... Inborn errors of carbohydrate, ammonia, amino acid, and organic acid metabolism. In: Gleason CA, Sawyer T, eds. Avery's Diseases of the Newborn . 11th ed. Philadelphia, PA: Elsevier; ...
    https://medlineplus.gov/ency/article/000373.htm - Medical Encyclopedia
  5. Alkaptonuria 
    ... Inborn errors of carbohydrate, ammonia, amino acid, and organic acid metabolism. In: Gleason CA, Sawyer T, eds. Avery's Diseases of the Newborn . 11th ed. Philadelphia, PA: Elsevier; ...
    https://medlineplus.gov/ency/article/001200.htm - Medical Encyclopedia
  6. Propionic acidemia 
    ... lipids (fats) properly. It is classified as an organic acid disorder, which is a condition that leads to an abnormal buildup of particular acids known as organic acids. Abnormal levels of organic acids in the ...
    https://medlineplus.gov/genetics/condition/propionic-acidemia - Genetics
  7. Maple syrup urine disease 
    ... SC, Campeau PM, Lee BH. Branched-chain amino acid metabolism: from rare Mendelian diseases to more common disorders. Hum Mol Genet. 2014 ...
    https://medlineplus.gov/genetics/condition/maple-syrup-urine-disease - Genetics
  8. Methylmalonic acidemia 
    ... is a buildup of a substance called methylmalonic acid in the blood. This condition is passed down through families. It is one of several conditions called an "inborn error of metabolism."
    https://medlineplus.gov/ency/article/001162.htm - Medical Encyclopedia
  9. Hereditary urea cycle abnormality 
    ... Blood ammonia Blood glucose Plasma amino acids Urine organic acids Genetic tests Liver biopsy MRI or CT scan ... diseases, there is no way to prevent these disorders from ... to follow the prescribed diet can help prevent severe illness.
    https://medlineplus.gov/ency/article/000372.htm - Medical Encyclopedia
  10. Opisthotonos 
    ... Douglas, and Bennett's Principles and Practice of Infectious Diseases. 9th ed. Philadelphia, PA: Elsevier; 2020:chap 244. Kliegman RM, St. Geme JW, Blum NJ, et al. Defects in metabolism of amino acids. In: Kliegman RM, St. Geme JW, Blum NJ, ...
    https://medlineplus.gov/ency/article/003195.htm - Medical Encyclopedia
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