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  2. Medium-chain acyl-coenzyme A dehydrogenase deficiency

    en.wikipedia.org/wiki/Medium-chain_acyl-coenzyme...

    The MCADD disorder is commonly mistaken for Reye Syndrome by pediatricians. Reye Syndrome is a severe disorder that may develop in children while they appear to be recovering from viral infections such as chicken pox or flu. Most cases of Reye Syndrome are associated with the use of Aspirin during these viral infections.

  3. Very long-chain acyl-coenzyme A dehydrogenase deficiency

    en.wikipedia.org/wiki/Very_long-chain_acyl...

    Treatment and management of VLCAD deficiency involve dietary restrictions as well as implementation of proper hydration to avoid further complications. Hospitalization due to VLCAD deficiency can be treated with intravenous (IV) glucose for hydration and alkalization of urine and prevention of renal malfunction or failure. [ 10 ]

  4. Short-chain acyl-coenzyme A dehydrogenase deficiency

    en.wikipedia.org/wiki/Short-chain_acyl-coenzyme...

    Treatment Intravenous fluids/ high dextrose concentration [ 5 ] Short-chain acyl-coenzyme A dehydrogenase deficiency (SCADD) is an autosomal recessive [ 6 ] fatty acid oxidation disorder which affects enzymes required to break down a certain group of fats called short chain fatty acids .

  5. Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

    en.wikipedia.org/wiki/Long-chain_3-hydroxyacyl...

    Diagnoses are typically made based on newborn screening done from blood obtained using a heel prick at birth. Prior to widespread inclusion of FAO (fatty acid oxidation) disorders in newborn screening tests, diagnosis typically occurred as a result of children presenting for medical attention having hypoglycemic hypoketotic crisis.

  6. Inborn errors of metabolism - Wikipedia

    en.wikipedia.org/wiki/Inborn_errors_of_metabolism

    In the middle of the 20th century the principal treatment for some of the amino acid disorders was restriction of dietary protein and all other care was simply management of complications. In the past twenty years, new medications, enzyme replacement, gene therapy, and organ transplantation have become available and beneficial for many ...

  7. Sudden unexplained death in childhood - Wikipedia

    en.wikipedia.org/wiki/Sudden_Unexplained_Death...

    The causes of SIDS and SUDC are not definitively known but there are good chances heart arrhythmias and seizures are the main causes. Although it can happen to any child under the age of 18 (after which the deaths are classified as Sudden arrhythmic death syndrome (SADS)), it is most common in those aged between 1–4 years, where according to ...

  8. 3-hydroxyacyl-coenzyme A dehydrogenase deficiency - Wikipedia

    en.wikipedia.org/wiki/3-hydroxyacyl-coenzyme_A...

    Problems related to 3-hydroxyacyl-coenzyme A dehydrogenase deficiency can be triggered by periods of fasting or by illnesses such as viral infections. This disorder is sometimes mistaken for Reye syndrome, a severe disorder that may develop in children while they appear to be recovering from viral infections such as chicken pox or flu. Most ...

  9. Fatty-acid metabolism disorder - Wikipedia

    en.wikipedia.org/wiki/Fatty-acid_metabolism_disorder

    The primary treatment method for fatty-acid metabolism disorders is dietary modification. It is essential that the blood-glucose levels remain at adequate levels to prevent the body from moving fat to the liver for energy. This involves snacking on low-fat, high-carbohydrate nutrients every 2–6 hours.