Hypoglycemia of infancy and childhood

Stephen Lafranchi

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

Hypoglycemia of infancy and childhood represents a treatable cause of mental retardation and seizures. Most neonates with hypoglycemia have transient disorders, but with persistent hypoglycemia one must consider hyperinsulinism, hypopituitarism, or hereditary hepatic enzyme deficiencies. Outside of the neonatal period, ketotic hypoglycemia is the most common cause of hypoglycemia in childhood. One cannot overemphasize the value of obtaining certain diagnostic tests at the presentation of spontaneous hypoglycemia, including blood for insulin, cortisol, growth hormone, and urine for ketone bodies. Supportive treatment with intravenous glucose to maintain the blood glucose greater than 50 mg/dl is important until a diagnosis is established allowing specific therapy aimed at the underlying disorder.

Original languageEnglish (US)
Pages (from-to)961-982
Number of pages22
JournalPediatric Clinics of North America
Volume34
Issue number4
StatePublished - 1987

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Hypoglycemia
Ketone Bodies
Hypopituitarism
Hyperinsulinism
Routine Diagnostic Tests
Intellectual Disability
Growth Hormone
Hydrocortisone
Blood Glucose
Seizures
Urine
Insulin
Glucose
Liver
Enzymes

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Hypoglycemia of infancy and childhood. / Lafranchi, Stephen.

In: Pediatric Clinics of North America, Vol. 34, No. 4, 1987, p. 961-982.

Research output: Contribution to journalArticle

Lafranchi, S 1987, 'Hypoglycemia of infancy and childhood', Pediatric Clinics of North America, vol. 34, no. 4, pp. 961-982.
Lafranchi, Stephen. / Hypoglycemia of infancy and childhood. In: Pediatric Clinics of North America. 1987 ; Vol. 34, No. 4. pp. 961-982.
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