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Results 1 - 10 of 32 for Severe lactic acidosis
  1. Pyruvate carboxylase deficiency 
    ... mostly in Europe, particularly France. Affected infants have severe lactic acidosis, a buildup of ammonia in the blood (hyperammonemia), ...
    https://medlineplus.gov/.../pyruvate-carboxylase-deficiency - Genetics
  2. Pearson syndrome 
    ... die in infancy or early childhood due to severe lactic acidosis or liver failure. Many of those who survive ...
    https://medlineplus.gov/genetics/condition/pearson-syndrome - Genetics
  3. Mitochondrial complex I deficiency 
    ... cause nausea, vomiting, weakness, and rapid breathing. In severe cases, lactic acidosis can be life-threatening.People with mitochondrial complex ...
    https://medlineplus.gov/.../mitochondrial-complex-i-deficiency - Genetics
  4. Dihydrolipoamide dehydrogenase deficiency 
    ... life-threatening buildup of lactic acid in tissues (lactic acidosis), which can cause nausea, vomiting, severe breathing problems, and an abnormal heartbeat. Neurological problems ...
    https://medlineplus.gov/...dihydrolipoamide-dehydrogenase-deficiency - Genetics
  5. Pyruvate dehydrogenase deficiency 
    ... a potentially life-threatening buildup of lactic acid (lactic acidosis), which can cause nausea, vomiting, severe breathing problems, and an abnormal heartbeat. People with ...
    https://medlineplus.gov/.../pyruvate-dehydrogenase-deficiency - Genetics
  6. BOLA3 gene 
    ... the glycine cleavage system. Affected infants often have severe brain dysfunction (encephalopathy) and elevated levels of a chemical called lactic acid in the body (lactic acidosis). These babies usually do not survive past infancy. ...
    https://medlineplus.gov/genetics/gene/bola3 - Genetics
  7. NFU1 gene 
    ... the glycine cleavage system. Affected infants often have severe brain dysfunction (encephalopathy) and elevated levels of a chemical called lactic acid in the body (lactic acidosis). These babies usually do not survive past infancy. ...
    https://medlineplus.gov/genetics/gene/nfu1 - Genetics
  8. GRACILE syndrome 
    GRACILE syndrome is a severe disorder ... is slow (intrauterine growth retardation). Affected newborns are smaller than average ...
    https://medlineplus.gov/genetics/condition/gracile-syndrome - Genetics
  9. MT-TE gene 
    ... the first few months of life and causes severe muscle weakness, poor muscle tone (hypotonia), and buildup of a chemical called lactic acid in the body (lactic acidosis). Affected infants often have difficulty feeding and need ...
    https://medlineplus.gov/genetics/gene/mt-te - Genetics
  10. DLD gene 
    ... dehydrogenase deficiency. The signs and symptoms of this severe condition vary widely, but they most commonly include a potentially life-threatening buildup of lactic acid in the tissues (lactic acidosis), neurological problems, and liver disease.Most DLD mutations ...
    https://medlineplus.gov/genetics/gene/dld - Genetics
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