Morphological mosaicism of the pancreatic islets: A novel anatomopathological form of persistent hyperinsulinemic hypoglycemia of infancy

Journal of Clinical Endocrinology and Metabolism

Volumn 96, Issue 12, 2011, Pages 3785-3793

  Sempoux, C ^a   Capito, C ^b,c   Bellanne Chantelot C ^d   Verkarre, V ^b   De Lonlay, P ^b   Aigrain, Y ^b   Fekete, C ^b   Guiot, Y ^a   Rahier, Jacques ^a  

^a CLINIQUES UNIVERSITAIRES SAINT LUC   (Belgium)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c INSERM   (France)

^d ASSISTANCE PUBLIQUE HÔPITAUX DE PARIS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE SENSITIVE POTASSIUM CHANNEL; DIAZOXIDE;

ABCC8 GENE; ARTICLE; BIRTH WEIGHT; CELL COMPOSITION; CELL ENLARGEMENT; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; DISEASE COURSE; FEMALE; GCK GENE; GENE; GENE DELETION; GENE MUTATION; GOLGI COMPLEX; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPOGLYCEMIA; INFANT; INSULIN SYNTHESIS; KCNJ11 GENE; MALE; MORPHOLOGICAL TRAIT; MOSAICISM; PANCREAS ISLET; PANCREAS ISLET BETA CELL; PANCREAS RESECTION; PATHOLOGICAL ANATOMY; PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; PRIORITY JOURNAL;

FEMALE; HUMANS; INFANT; INFANT, NEWBORN; ISLETS OF LANGERHANS; MALE; MICROSATELLITE REPEATS; MOSAICISM; MUTATION; PANCREATECTOMY; PERSISTENT HYPERINSULINEMIA HYPOGLYCEMIA OF INFANCY; TREATMENT OUTCOME;

EID: 83155168493     PISSN: 0021972X     EISSN: 19457197     Source Type: Journal    
DOI: 10.1210/jc.2010-3032     Document Type: Article

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