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Clinical Pediatrics
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Persistent Neonatal Hyperinsulinism

P.M. Mathew

From the Departments of Paediatrics, Surgery and Pathology, Dhahran Health Center, Dhahran, Saudi Arabia

J.M. Young

From the Departments of Paediatrics, Surgery and Pathology, Dhahran Health Center, Dhahran, Saudi Arabia

Y.K. Abu-Osba

From the Departments of Paediatrics, Surgery and Pathology, Dhahran Health Center, Dhahran, Saudi Arabia

B.D. Mulhern

From the Departments of Paediatrics, Surgery and Pathology, Dhahran Health Center, Dhahran, Saudi Arabia

S. Hammoudi

From the Departments of Paediatrics, Surgery and Pathology, Dhahran Health Center, Dhahran, Saudi Arabia

J.A. Hamdan

From the Departments of Paediatrics, Surgery and Pathology, Dhahran Health Center, Dhahran, Saudi Arabia

A.R. Sa'di

From the Departments of Paediatrics, Surgery and Pathology, Dhahran Health Center, Dhahran, Saudi Arabia

Over a 3-year period, the diagnosis of persistent neonatal hyperinsulinism (PNH) was made in seven infants, from an unselected cohort of 18,726 births, all of Saudi Arabian origin. Thus the incidence of PNH was one in 2,675 births. The high incidence, associated consanguinity, and occurrence in siblings suggest that PNH may be inherited as an autosomal recessive disorder.

Clinical Pediatrics, Vol. 27, No. 3, 148-151 (1988)
DOI: 10.1177/000992288802700307


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