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4,623 Possible Causes for Diffuse Hepatic Steatosis, Hypoglycemia, Muscle Hypotonia

  • Reye Syndrome

    In Reye-like syndrome, because of inborn errors of metabolism, hypoglycemia, hypoketonemia, elevated ammonia, and organic aciduria are often evident.[] Abstract Analysis of the liver histopathology in 19 children with clinical Reye syndrome (RS) revealed that nine had diffuse panlobular steatosis, one giant cell hepatitis[] Laboratory evaluation revealed initial hypoglycemia, and markedly elevated liver enzymes, prolonged clotting times, and elevated ammonia levels.[]

  • Carnitine Transporter Deficiency

    Infants often present with hypoketotic hypoglycemia, poor feeding, irritability, lethargy, and hepatomegaly, triggered by fasting stress or common illnesses including gastoenteritis[] Children with the childhood myopathic (cardiac) type usually present between ages two to four with heart disease (cardiomyopathy), low muscle tone (hypotonia), skeletal muscle[] Carbohydrate intake before bedtime can help in reducing morning hypoglycemia.[]

    Missing: Diffuse Hepatic Steatosis
  • Glycogen Storage Disease Type 4

    Meticulous adherence to a dietary regimen may reduce liver size, prevent hypoglycemia, reduce symptoms, and allow for growth and development.[] Clinical features are muscle hypotonia and cirrhosis. Death from liver disease usually occurs before age 2.[] Blood glucose levels will depict a picture of hypoglycemia as there is excess of glycogen circulating in the body but poor amount of usable glucose.[]

    Missing: Diffuse Hepatic Steatosis
  • Glycogen Storage Disease Type 2

    Although there are no reports in the literature of drugs precipitating hypoglycemia in children with GSD III, drugs known to cause hypoglycemia should be avoided.[] […] deficiency; large amounts of glycogen accumulate in the lysosomes of skeletal muscle, heart, liver, spinal cord, and brain; three forms have been described: the infantile[] hypotonia respiratory distress Juvenile and adult form skeletal myopathy delayed-gross motor development limb-girdle weakness respiratory issues Enzyme replacement therapy[]

    Missing: Diffuse Hepatic Steatosis
  • Glycogen Storage Disease Type 3

    During periods of hypoglycemia, Cori disease is treated with frequent high carbohydrate meals with cornstarch supplements.[] The first signs and symptoms are typically poor muscle tone (hypotonia) and mild myopathy in early childhood. The myopathy may become severe by early to mid-adulthood.[] Clinically, patients with GSD III present in infancy or early childhood with hepatomegaly, hypoglycemia, and growth retardation.[]

    Missing: Diffuse Hepatic Steatosis
  • Propionic Acidemia

    It is frequently accompanied by metabolic acidosis with anion gap, ketonuria, hypoglycemia, hyperammonemia, and cytopenias.[] Clinical presentation was with acute aphasia, generalized hypotonia, and muscle weakness.[] Mobilization of free fatty acids from stores in the liver in response to the hypoglycemia produces a fatty liver.[]

    Missing: Diffuse Hepatic Steatosis
  • Cannabis Abuse

    This is particularly risky for diabetics taking oral medications or insulin, as hyperglycemia or hypoglycemia can be fatal.[]

    Missing: Diffuse Hepatic Steatosis
  • Methylmalonic Acidemia

    […] affecting the catabolism of propionic acid, is manifested by persistent metabolic acidosis, urinary excretion of large amounts of methylmalonic acid, and occasionally by hypoglycemia[] 8), muscle hypotonia (n 8), recurrent vomiting (n 4), tremor (n 2), ataxia (n 2), and abnormal posture (n 1).The onset age of seizure ranged from 8 days to 11 years.[] Hypoglycemia is a frequent manifestation of MMA.[]

    Missing: Diffuse Hepatic Steatosis
  • Maple Syrup Urine Disease

    Abstract Extract : We are reporting a patient with classic, thiamine-unresponsive maple syrup urine disease (MSUD) associated with severe fasting hypoglycemia.[] […] rigidity) and hypotonia (muscle limpness) high-pitched cry Signs of intermediate and thiamine-response MSUD include: seizures neurological deficiencies developmental delays[] Signs and symptoms of Maple Syrup Urine Disease are: Poor feeding, lack of energy (lethargy) Vomiting Poor muscle tone (hypotonia) Developmental delay Backward arching of[]

    Missing: Diffuse Hepatic Steatosis
  • Accidental Hypothermia

    […] the external auditory meatus, inaccuracy of infrared-based thermometers, iatrogenic trauma to the femoral vessels, chronic/terminal comorbidities, poisonings, pregnancy, hypoglycemia[] Best Review Article accidentalhypothermia Back to top Predisposing factors hypoglycemia, malnutrition, ETOH, Addison’s, infection, and Myxedema (especially if failure to rewarm[] Hypoglycemia can cause mild hypothermia. • Coagulation studies: Hypothermia directly affects coagulation through several mechanisms.[]

    Missing: Diffuse Hepatic Steatosis

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