Genetic hyperinsulinism. Medical search. Frequent questions

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Anatomy4

Chromosomes, Human, Pair 11 Islets of Langerhans Insulin-Secreting Cells Pancreas

Diseases13

Congenital Hyperinsulinism Hyperinsulinism Hypoglycemia Hyperammonemia Insulinoma Beckwith-Wiedemann Syndrome Congenital Disorders of Glycosylation Hyperandrogenism Hamartoma Pancreatic Neoplasms Hypopituitarism Seizures Syndrome

Chemicals and Drugs22

Sulfonylurea Receptors Receptors, Drug Potassium Channels, Inwardly Rectifying Diazoxide Glutamate Dehydrogenase ATP-Binding Cassette Transporters Insulin KATP Channels Insulin Antibodies Sulfonylurea Compounds 3-Hydroxyacyl CoA Dehydrogenases Potassium Channels Cyclin-Dependent Kinase Inhibitor p57 Tolbutamide Blood Glucose Chlorthalidone Octreotide Proinsulin C-Peptide Ammonia Adenosine Triphosphate Glucose

Analytical, Diagnostic and Therapeutic Techniques and Equipment4

Diagnostic Techniques, Endocrine Pancreatectomy Pedigree Glucose Tolerance Test

Phenomena and Processes8

Mutation Chromosomes, Human, Pair 11 Mutation, Missense Heterozygote Mosaicism Genes, Dominant Homozygote Point Mutation

Named Groups1

Infant, Newborn

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Named Groups

Congenital Hyperinsulinism Hyperinsulinism Sulfonylurea Receptors Receptors, Drug Potassium Channels, Inwardly Rectifying Diazoxide Hypoglycemia Diagnostic Techniques, Endocrine Hyperammonemia Glutamate Dehydrogenase ATP-Binding Cassette Transporters Pancreatectomy Insulin Insulinoma KATP Channels Insulin Antibodies Sulfonylurea Compounds Beckwith-Wiedemann Syndrome 3-Hydroxyacyl CoA Dehydrogenases Potassium Channels Infant, Newborn Congenital Disorders of Glycosylation Cyclin-Dependent Kinase Inhibitor p57 Mutation Chromosomes, Human, Pair 11 Islets of Langerhans Tolbutamide Insulin-Secreting Cells Hyperandrogenism Blood Glucose Mutation, Missense Chlorthalidone Octreotide Proinsulin Pancreas Hamartoma C-Peptide Heterozygote Mosaicism Pancreatic Neoplasms Hypopituitarism Pedigree Ammonia Seizures Genes, Dominant Syndrome Adenosine Triphosphate Glucose Homozygote Glucose Tolerance Test Point Mutation

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