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Article

Loss of imprinted genes and paternal SUR1 mutations lead to focal form of congenital hyperinsulinism.

Hormone research - 1 Jan 2000

Fournet J C, Mayaud C, de Lonlay P, Verkarre V, Rahier J, Brunelle F, Robert J J, Nihoul-Fékété C, Saudubray J M, Junien C

Abstract excerpt

Persistent hyperinsulinaemic hypoglycaemia of infancy (PHHI) is a heterogeneous disorder characterized by profound hypoglycaemia due to inappropriate hypersecretion of insulin. An important diagnostic goal is to distinguish patients with a focal hyperplasia of islet cells of the pancreas (FoPHHI) from those with a diffuse abnormality of islets (DiPHHI), because the management differs significantly. The intriguing...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 10895035
DOI: 10.1159/000053197

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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