hypoglycemia/uppköst

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The prevalence of hypoglycemia in children with vomiting or decreased oral intake and irritability.

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OBJECTIVE This study aimed to estimate the prevalence of hypoglycemia in children younger than 5 years presenting to the emergency department with vomiting or decreased oral intake and irritability. METHODS Children aged 1 month to 5 years presenting to the emergency department with vomiting (twice

Identification of 5-hydroxyhexanoic acid in the urine of twin siblings with a Reye's-like syndrome associated with dicarboxylic aciduria and hypoglycaemia and with similarities to Jamaican vomiting sickness.

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Twin male infant siblings who presented in Harrow, UK, with a Reye's-like syndrome associated with profound hypoglycaemia, vomiting, diarrhoea, coma and death in one child, with dicarboxylic aciduria, and similarities to Jamacian vomiting sickness (hypoglycin toxicity) have been shown to excrete

A 36-year-old man with vomiting, pain abdomen, significant weight loss, hyponatremia, and hypoglycemia.

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Diagnosis of Strongyloides stercoralis hyperinfection can be a challenge. The key to a timely diagnosis is to have a high index of suspicion. We present a rare case of a 36-year-old human immunodeficiency virus negative male patient, who was on multidrug therapy for lepromatous leprosy and was

Toxic hypoglycaemia (Jamaican vomiting sickness). First case reported from the territory of Trinidad and Tobago.

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Acute toxic hypoglycaemia occurring in the vomiting sickness of Jamaica; clinical aspects.

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Acute toxic hypoglycaemia occurring in the vomiting sickness of Jamaica; morbid anatomical aspects.

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Dicarboxylic aciduria as an indicator of defective beta-oxidation in twin siblings with a vomiting sickness and hypoglycaemia similar to Jamaican vomiting sickness [proceedings].

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Twin siblings with a Reye's-like syndrome associated with an abnormal organic aciduria, hypoglycemia, diarrhea, and vomiting with close similarities to Jamaican vomiting sickness.

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[Hypoglycemia in the child and its relation with acetonemic vomiting].

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Acute toxic hypoglycaemia in the vomiting sickness of Jamaica.

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A 20-year-old man with recurrent abdominal pain and vomiting since the age of 5 years. Familial chronic pancreatitis with nesidioblastosis and hyperinsulinaemic hypoglycaemia.

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[Carbohydrate metabolism disorders in childhood; hypoglycemias and periodic vomiting with acetonuria].

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Hypoglycemia-occipital syndrome: a specific neurologic syndrome following neonatal hypoglycemia?

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This study attempted to elaborate the existence of a specific neurologic pattern observed in children who experienced neonatal hypoglycemia. Twenty-seven patients with seizure and history of neonatal hypoglycemia were compared with 28 children suffering from idiopathic occipital epilepsy. In both

[Assessment of the natural history and clinical presentation of acetonemic vomiting].

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BACKGROUND Ketosis in children may result from physiological adaptation to situations like fasting, fat-rich diet, straining physical activity, as well as from serious endocrine or metabolic disorders. The most frequently diagnosed cause of ketoacidosis are states of acetonemia and acetonuria with

[Persistent neonatal hypoglycemia in nesidioblastosis of the pancreas].

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A now 10 month old female infant suffered from persistent non ketotic neonatal hypoglycemia despite continuous intravenous application of glucose (greater than 10 mg/kg/min). There was only a transient response of blood glucose after intravenous administration of glucagon and prednisolon.

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