Clinical characteristics and phenotype-genotype review of 25 Omani children with congenital hyperinsulinism in infancy. A one-decade single-center experience. [electronic resource]
Producer: 20200117Description: 669-674 p. digitalISSN:- 1658-3175
- Apnea -- etiology
- Child, Preschool
- Congenital Hyperinsulinism -- genetics
- Diabetes Mellitus -- drug therapy
- Enzyme Replacement Therapy
- Exocrine Pancreatic Insufficiency -- drug therapy
- Female
- Gastrointestinal Agents -- therapeutic use
- Heterozygote
- Homozygote
- Humans
- Hypoglycemia -- complications
- Infant
- Infant, Newborn
- Lethargy -- etiology
- Male
- Mutation
- Octreotide -- therapeutic use
- Oman
- Pancreatectomy
- Peptides, Cyclic -- therapeutic use
- Postoperative Complications -- drug therapy
- Retrospective Studies
- Seizures -- etiology
- Sirolimus -- therapeutic use
- Somatostatin -- analogs & derivatives
- Sulfonylurea Receptors -- genetics
- Treatment Outcome
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Publication Type: Journal Article
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