Prenatal diagnosis and postnatal management of diffuse congenital hyperinsulinism: A case report

Fetal Diagnosis and Therapy

Volumn 21, Issue 6, 2006, Pages 515-518

  Peranteau, William H ^a   Ganguly, Arupa ^a   Steinmuller, Laura ^a   Thornton, Paul ^a   Johnson, Mark P ^a   Howell, Lori J ^a   Stanley, Charles A ^a   Adzick, N Scott ^a,b  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

Hyperinsulinism; Hypoglycemia; Kir6.2; Prenatal diagnosis; SUR1

Indexed keywords

ADULT; AMNIOCENTESIS; ARTICLE; CASE REPORT; CESAREAN SECTION; DIAGNOSTIC VALUE; DIFFUSE CONGENITAL HYPERINSULINISM; FEMALE; GENE; GENE IDENTIFICATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC SUSCEPTIBILITY; GESTATION PERIOD; GLYCEMIC CONTROL; HUMAN; HUMAN TISSUE; HYPOGLYCEMIA; MALE; MUTATIONAL ANALYSIS; NEWBORN; PANCREAS RESECTION; PERINATAL PERIOD; PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SUR1 GENE; TREATMENT FAILURE;

AMNIOCENTESIS; ATP-BINDING CASSETTE TRANSPORTERS; FEMALE; HUMANS; INFANT, NEWBORN; MALE; PANCREATECTOMY; PERSISTENT HYPERINSULINEMIA HYPOGLYCEMIA OF INFANCY; POTASSIUM CHANNELS; POTASSIUM CHANNELS, INWARDLY RECTIFYING; PREGNANCY; RECEPTORS, DRUG;

EID: 33751330402     PISSN: 10153837     EISSN: None     Source Type: Journal    
DOI: 10.1159/000095664     Document Type: Article

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