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Results 1 - 10 of 14 for Recurrent hypoglycemia
  1. Leukoencephalopathy with thalamus and brainstem involvement and high lactate 
    ... F. EARS2 mutations cause fatal neonatal lactic acidosis, recurrent hypoglycemia and agenesis of corpus callosum. Metab Brain Dis. ...
    https://medlineplus.gov/...nd-brainstem-involvement-and-high-lactate - Genetics
  2. Silver-Russell syndrome 
    ... children often have difficulty feeding. Some children develop recurrent episodes of low blood glucose (hypoglycemia). Gastrointestinal problems, such as vomiting and a backflow ...
    https://medlineplus.gov/genetics/condition/silver-russell-syndrome - Genetics
  3. Glycogen storage disease type 0 
    ... Nishino I. Muscle glycogen storage disease 0 presenting recurrent syncope with ... recognized cause of ketotic hypoglycemia. Mol Genet Metab. 2006 Apr;87(4):284- ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-0 - Genetics
  4. Familial glucocorticoid deficiency 
    ... to seizures, learning difficulties, and other neurological problems. Hypoglycemia that is left untreated for prolonged periods can lead to neurological damage and death. Other features of familial glucocorticoid deficiency can include recurrent infections and skin coloring darker than that of ...
    https://medlineplus.gov/.../familial-glucocorticoid-deficiency - Genetics
  5. Dihydrolipoamide dehydrogenase deficiency 
    ... symptom. The liver problems are usually associated with recurrent vomiting and abdominal ... the signs and symptoms of dihydrolipoamide dehydrogenase ...
    https://medlineplus.gov/...dihydrolipoamide-dehydrogenase-deficiency - Genetics
  6. Combined pituitary hormone deficiency 
    ... jaundice), low levels of glucose in the blood (hypoglycemia), and genital ... seizures (epilepsy), and developmental delays. Some affected individuals ...
    https://medlineplus.gov/.../combined-pituitary-hormone-deficiency - Genetics
  7. Donohue syndrome 
    ... nostrils, and low-set ears. Affected individuals develop recurrent, life-threatening infections beginning in infancy.Donohue syndrome ...
    https://medlineplus.gov/genetics/condition/donohue-syndrome - Genetics
  8. Carnitine palmitoyltransferase II deficiency 
    ... for energy. Together, these signs are called hypoketotic hypoglycemia. If affected individuals fast for long periods of ... life. This form involves recurring episodes of hypoketotic hypoglycemia, seizures, liver dysfunction, cardiomyopathy, arrhythmia, and muscle weakness ( ...
    https://medlineplus.gov/...nitine-palmitoyltransferase-ii-deficiency - Genetics
  9. Very long-chain acyl-CoA dehydrogenase deficiency 
    ... can have low blood sugar (glucose), known as hypoglycemia. Affected individuals are also at risk for serious ... symptoms of the disorder such as lethargy and hypoglycemia. Very long-chain fatty acids or partially metabolized ...
    https://medlineplus.gov/...g-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  10. Glycogen storage disease type I 
    ... newborns. Affected infants may have low blood sugar (hypoglycemia), which can lead to seizures. They can also ... cells (neutropenia), which can make them prone to recurrent bacterial infections. Neutropenia is usually apparent by age ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-i - Genetics
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