Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy

Journal of Clinical Investigation

Volumn 100, Issue 4, 1997, Pages 802-807

  De Lonlay, Pascale ^a   Fournet, Jean Christophe ^a,b   Rahier, Jacques ^c   Gross Morand, Marie Sylvie ^a   Poggi Travert, Florence ^b   Foussier, Valérie ^b   Bonnefont, Jean Paul ^a   Brusset, Marie Claire ^b   Brunelle, Francis ^b   Robert, Jean Jacques ^b   Nihoul Fékété, Claire ^b   Saudubray, Jean Marie ^b   Junien, Claudine ^a,b  

^a INSERM   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c CLINIQUES UNIVERSITAIRES SAINT LUC   (Belgium)

Author keywords

Beckwith Wiedemann syndrome; Hyperinsulinism; Loss of alleles; Nesidioblastosis; Potassium channel

Indexed keywords

DIAZOXIDE;

ARTICLE; CHROMOSOME 11P; CHROMOSOME LOSS; CLINICAL ARTICLE; FEMALE; GENE DELETION; HUMAN; HUMAN TISSUE; INFANT; INSULINOMA; MALE; NEWBORN; PANCREAS ISLET CELL HYPERPLASIA; PANCREAS ISLET DISEASE; PANCREAS RESECTION; PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; PRIORITY JOURNAL;

EID: 0030880778     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI119594     Document Type: Article

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